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 15 42115152 42115152 + Silent SNP C C T TCGA-OR-A5JV-01A-11D-A29I-10 TCGA-OR-A5JV-10A-01D-A29L-10 g.chr15:42115152C>T c.3348C>T c.(3346-3348)tcC>tcT p.S1116S ACC 15 42116197 42116197 + Missense_Mutation SNP C C T TCGA-OR-A5KB-01A-11D-A30A-10 TCGA-OR-A5KB-11A-11D-A30A-10 g.chr15:42116197C>T c.4169C>T c.(4168-4170)cCt>cTt p.P1390L BLCA 15 42067506 42067506 + Silent SNP G G A TCGA-YF-AA3M-01A-11D-A42E-08 TCGA-YF-AA3M-10D-01D-A42H-08 g.chr15:42067506G>A c.33G>A c.(31-33)cgG>cgA p.R11R BLCA 15 42092064 42092064 + Missense_Mutation SNP G G T TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:42092064G>T c.158G>T c.(157-159)aGa>aTa p.R53I BLCA 15 42092078 42092078 + Missense_Mutation SNP G G A TCGA-G2-A2EO-01A-11D-A17V-08 TCGA-G2-A2EO-11A-21D-A17V-08 g.chr15:42092078G>A c.172G>A c.(172-174)Gac>Aac p.D58N BLCA 15 42103140 42103140 + Missense_Mutation SNP C C T TCGA-UY-A78N-01A-12D-A339-08 TCGA-UY-A78N-10A-01D-A339-08 g.chr15:42103140C>T c.266C>T c.(265-267)tCc>tTc p.S89F BLCA 15 42107900 42107900 + Missense_Mutation SNP G G A TCGA-DK-A1A3-01A-11D-A13W-08 TCGA-DK-A1A3-10A-01D-A13W-08 g.chr15:42107900G>A c.1414G>A c.(1414-1416)Gat>Aat p.D472N BLCA 15 42109190 42109190 + Silent SNP G G A TCGA-UY-A9PF-01A-11D-A38G-08 TCGA-UY-A9PF-10A-01D-A38J-08 g.chr15:42109190G>A c.1686G>A c.(1684-1686)acG>acA p.T562T BLCA 15 42110219 42110219 + Silent SNP C C T TCGA-XF-AAML-01A-11D-A42E-08 TCGA-XF-AAML-10A-01D-A42H-08 g.chr15:42110219C>T c.1935C>T c.(1933-1935)atC>atT p.I645I BLCA 15 42113042 42113042 + Missense_Mutation SNP G G A TCGA-FD-A3SJ-01A-12D-A22Z-08 TCGA-FD-A3SJ-10A-01D-A22Z-08 g.chr15:42113042G>A c.2512G>A c.(2512-2514)Gtg>Atg p.V838M BLCA 15 42116052 42116052 + Missense_Mutation SNP G G A TCGA-K4-A5RJ-01A-11D-A289-08 TCGA-K4-A5RJ-10A-01D-A289-08 g.chr15:42116052G>A c.4024G>A c.(4024-4026)Gag>Aag p.E1342K BLCA 15 42116199 42116199 + Nonsense_Mutation SNP G G T TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr15:42116199G>T c.4171G>T c.(4171-4173)Gag>Tag p.E1391* BLCA 15 42117464 42117464 + Missense_Mutation SNP G G A TCGA-XF-A9T5-01A-11D-A42E-08 TCGA-XF-A9T5-10A-01D-A42H-08 g.chr15:42117464G>A c.4375G>A c.(4375-4377)Gac>Aac p.D1459N BRCA 15 42104263 42104263 + Missense_Mutation SNP G G A TCGA-AR-A0U3-01A-11D-A10G-09 TCGA-AR-A0U3-10A-01D-A10G-09 g.chr15:42104263G>A c.436G>A c.(436-438)Gcc>Acc p.A146T BRCA 15 42104774 42104774 + Missense_Mutation SNP G G A TCGA-BH-A0W7-01A-11D-A10Y-09 TCGA-BH-A0W7-10A-01D-A110-09 g.chr15:42104774G>A c.559G>A c.(559-561)Gag>Aag p.E187K BRCA 15 42110267 42110267 + Silent SNP C C T TCGA-BH-A0HA-01A-11D-A12Q-09 TCGA-BH-A0HA-11A-31D-A12Q-09 g.chr15:42110267C>T c.1983C>T c.(1981-1983)gaC>gaT p.D661D BRCA 15 42111445 42111445 + Splice_Site SNP C C T TCGA-E9-A1N4-01A-11D-A14K-09 TCGA-E9-A1N4-10A-01D-A14K-09 g.chr15:42111445C>T c.2311C>T c.(2311-2313)Cac>Tac p.H771Y BRCA 15 42113197 42113197 + Silent SNP G G C TCGA-AR-A0TU-01A-31D-A10G-09 TCGA-AR-A0TU-10A-01D-A10G-09 g.chr15:42113197G>C c.2667G>C c.(2665-2667)tcG>tcC p.S889S BRCA 15 42114459 42114459 + Missense_Mutation SNP T T C TCGA-BH-A18G-01A-11D-A12B-09 TCGA-BH-A18G-10A-01D-A12B-09 g.chr15:42114459T>C c.3086T>C c.(3085-3087)aTc>aCc p.I1029T BRCA 15 42115323 42115323 + Silent SNP C C G TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:42115323C>G c.3519C>G c.(3517-3519)ctC>ctG p.L1173L BRCA 15 42115928 42115928 + Silent SNP C C T TCGA-E2-A153-01A-12D-A12B-09 TCGA-E2-A153-11A-31D-A12B-09 g.chr15:42115928C>T c.3900C>T c.(3898-3900)atC>atT p.I1300I BRCA 15 42115998 42115998 + Missense_Mutation SNP G G A TCGA-AC-A23H-01A-11D-A159-09 TCGA-AC-A23H-11A-12D-A17G-09 g.chr15:42115998G>A c.3970G>A c.(3970-3972)Gag>Aag p.E1324K CESC 15 42067565 42067565 + Missense_Mutation SNP G G A TCGA-FU-A3HY-01A-11D-A21Q-09 TCGA-FU-A3HY-10A-01D-A21Q-09 g.chr15:42067565G>A c.92G>A c.(91-93)cGa>cAa p.R31Q CESC 15 42107876 42107876 + Missense_Mutation SNP G G C TCGA-Q1-A73O-01A-11D-A32I-09 TCGA-Q1-A73O-10B-01D-A32I-09 g.chr15:42107876G>C c.1390G>C c.(1390-1392)Gag>Cag p.E464Q CESC 15 42116052 42116052 + Nonsense_Mutation SNP G G T TCGA-EK-A2RO-01A-11D-A18J-09 TCGA-EK-A2RO-10A-01D-A18J-09 g.chr15:42116052G>T c.4024G>T c.(4024-4026)Gag>Tag p.E1342* CHOL 15 42113096 42113096 + Missense_Mutation SNP C C T TCGA-ZH-A8Y5-01A-11D-A417-09 TCGA-ZH-A8Y5-10A-01D-A41A-09 g.chr15:42113096C>T c.2566C>T c.(2566-2568)Cgc>Tgc p.R856C COAD 15 42067544 42067544 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr15:42067544G>A c.71G>A c.(70-72)cGc>cAc p.R24H COAD 15 42103096 42103096 + Silent SNP G G A TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr15:42103096G>A c.222G>A c.(220-222)ttG>ttA p.L74L COAD 15 42103106 42103106 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:42103106C>T c.232C>T c.(232-234)Cgg>Tgg p.R78W COAD 15 42104313 42104313 + Silent SNP G G A TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr15:42104313G>A c.486G>A c.(484-486)gtG>gtA p.V162V COAD 15 42105244 42105244 + Missense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:42105244G>T c.764G>T c.(763-765)gGg>gTg p.G255V COAD 15 42105966 42105966 + Missense_Mutation SNP G G A TCGA-AA-3875-01A-01W-0900-09 TCGA-AA-3875-10A-01W-0902-09 g.chr15:42105966G>A c.985G>A c.(985-987)Gtc>Atc p.V329I COAD 15 42106899 42106899 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:42106899T>G c.1150T>G c.(1150-1152)Tcg>Gcg p.S384A COAD 15 42107484 42107484 + Nonsense_Mutation SNP C C T TCGA-AA-3875-01A-01W-0900-09 TCGA-AA-3875-10A-01W-0902-09 g.chr15:42107484C>T c.1216C>T c.(1216-1218)Cag>Tag p.Q406* COAD 15 42107495 42107496 + Frame_Shift_Ins INS - - C TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr15:42107495_42107496insC c.1227_1228insC c.(1228-1230)cccfs p.P410fs COAD 15 42107534 42107534 + Silent SNP C C T TCGA-D5-5537-01A-21D-1924-10 TCGA-D5-5537-10A-01D-1924-10 g.chr15:42107534C>T c.1266C>T c.(1264-1266)acC>acT p.T422T COAD 15 42110446 42110446 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:42110446C>A c.2053C>A c.(2053-2055)Ctc>Atc p.L685I COAD 15 42110446 42110446 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:42110446C>A c.2053C>A c.(2053-2055)Ctc>Atc p.L685I COAD 15 42111074 42111074 + Missense_Mutation SNP G G A TCGA-AA-3684-01A-02W-0900-09 TCGA-AA-3684-10A-01W-0900-09 g.chr15:42111074G>A c.2228G>A c.(2227-2229)cGt>cAt p.R743H COAD 15 42111476 42111476 + Missense_Mutation SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr15:42111476C>T c.2342C>T c.(2341-2343)cCg>cTg p.P781L COAD 15 42113251 42113251 + Silent SNP T T G TCGA-AA-A029-01A-01W-A00E-09 TCGA-AA-A029-10A-01W-A00E-09 g.chr15:42113251T>G c.2721T>G c.(2719-2721)acT>acG p.T907T COAD 15 42114550 42114550 + Frame_Shift_Del DEL C C - TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr15:42114550delC c.3177delC c.(3175-3177)agcfs p.S1059fs COAD 15 42115703 42115703 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:42115703C>T c.3675C>T c.(3673-3675)atC>atT p.I1225I COAD 15 42116162 42116162 + Silent SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42116162C>A c.4134C>A c.(4132-4134)ctC>ctA p.L1378L COAD 15 42116730 42116730 + Missense_Mutation SNP G G A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr15:42116730G>A c.4280G>A c.(4279-4281)cGc>cAc p.R1427H COADREAD 15 42067544 42067544 + Missense_Mutation SNP G G A TCGA-AA-3947-01A-01W-0995-10 TCGA-AA-3947-10A-01W-0995-10 g.chr15:42067544G>A c.71G>A c.(70-72)cGc>cAc p.R24H COADREAD 15 42103096 42103096 + Silent SNP G G A TCGA-AA-3850-01A-01W-0995-10 TCGA-AA-3850-10A-01W-0995-10 g.chr15:42103096G>A c.222G>A c.(220-222)ttG>ttA p.L74L COADREAD 15 42103106 42103106 + Missense_Mutation SNP C C T TCGA-AA-3864-01A-01W-0995-10 TCGA-AA-3864-10A-01W-0995-10 g.chr15:42103106C>T c.232C>T c.(232-234)Cgg>Tgg p.R78W COADREAD 15 42103107 42103107 + Missense_Mutation SNP G G A TCGA-AG-3727-01A-01W-0899-10 TCGA-AG-3727-10A-01W-0901-10 g.chr15:42103107G>A c.233G>A c.(232-234)cGg>cAg p.R78Q COADREAD 15 42104313 42104313 + Silent SNP G G A TCGA-G4-6293-01A-11D-1719-10 TCGA-G4-6293-10A-01D-1719-10 g.chr15:42104313G>A c.486G>A c.(484-486)gtG>gtA p.V162V COADREAD 15 42105244 42105244 + Missense_Mutation SNP G G T TCGA-AA-3663-01A-01D-1719-10 TCGA-AA-3663-11A-01D-1719-10 g.chr15:42105244G>T c.764G>T c.(763-765)gGg>gTg p.G255V COADREAD 15 42105966 42105966 + Missense_Mutation SNP G G A TCGA-AA-3875-01A-01W-0900-09 TCGA-AA-3875-10A-01W-0902-09 g.chr15:42105966G>A c.985G>A c.(985-987)Gtc>Atc p.V329I COADREAD 15 42106899 42106899 + Missense_Mutation SNP T T G TCGA-AA-3984-01A-02W-0995-10 TCGA-AA-3984-10A-01W-0999-10 g.chr15:42106899T>G c.1150T>G c.(1150-1152)Tcg>Gcg p.S384A COADREAD 15 42106934 42106934 + Frame_Shift_Del DEL G G - TCGA-AG-4008-01A-01W-1073-09 TCGA-AG-4008-10A-01W-1073-09 g.chr15:42106934delG c.1185delG c.(1183-1185)gtgfs p.V395fs COADREAD 15 42107484 42107484 + Nonsense_Mutation SNP C C T TCGA-AA-3875-01A-01W-0900-09 TCGA-AA-3875-10A-01W-0902-09 g.chr15:42107484C>T c.1216C>T c.(1216-1218)Cag>Tag p.Q406* COADREAD 15 42107495 42107496 + Frame_Shift_Ins INS - - C TCGA-AA-A00E-01A-01W-A005-10 TCGA-AA-A00E-10A-01W-A005-10 g.chr15:42107495_42107496insC c.1227_1228insC c.(1228-1230)cccfs p.P410fs COADREAD 15 42107532 42107532 + Missense_Mutation SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr15:42107532A>G c.1264A>G c.(1264-1266)Acc>Gcc p.T422A COADREAD 15 42107534 42107534 + Silent SNP C C T TCGA-D5-5537-01A-21D-1924-10 TCGA-D5-5537-10A-01D-1924-10 g.chr15:42107534C>T c.1266C>T c.(1264-1266)acC>acT p.T422T COADREAD 15 42110446 42110446 + Missense_Mutation SNP C C A TCGA-AA-A00N-01A-02W-A00E-09 TCGA-AA-A00N-10A-01W-A00E-09 g.chr15:42110446C>A c.2053C>A c.(2053-2055)Ctc>Atc p.L685I COADREAD 15 42110446 42110446 + Missense_Mutation SNP C C A TCGA-AZ-4315-01A-01D-1408-10 TCGA-AZ-4315-10A-01D-1408-10 g.chr15:42110446C>A c.2053C>A c.(2053-2055)Ctc>Atc p.L685I COADREAD 15 42111074 42111074 + Missense_Mutation SNP G G A TCGA-AA-3684-01A-02W-0900-09 TCGA-AA-3684-10A-01W-0900-09 g.chr15:42111074G>A c.2228G>A c.(2227-2229)cGt>cAt p.R743H COADREAD 15 42111476 42111476 + Missense_Mutation SNP C C T TCGA-AA-3662-01A-01D-1719-10 TCGA-AA-3662-11A-01D-1719-10 g.chr15:42111476C>T c.2342C>T c.(2341-2343)cCg>cTg p.P781L COADREAD 15 42113251 42113251 + Silent SNP T T G TCGA-AA-A029-01A-01W-A00E-09 TCGA-AA-A029-10A-01W-A00E-09 g.chr15:42113251T>G c.2721T>G c.(2719-2721)acT>acG p.T907T COADREAD 15 42114550 42114550 + Frame_Shift_Del DEL C C - TCGA-AA-3811-01A-01W-0995-10 TCGA-AA-3811-10A-01W-0995-10 g.chr15:42114550delC c.3177delC c.(3175-3177)agcfs p.S1059fs COADREAD 15 42115703 42115703 + Silent SNP C C T TCGA-AD-6889-01A-11D-1924-10 TCGA-AD-6889-10A-01D-1924-10 g.chr15:42115703C>T c.3675C>T c.(3673-3675)atC>atT p.I1225I COADREAD 15 42116162 42116162 + Silent SNP C C A TCGA-AA-A010-01A-01W-A00E-09 TCGA-AA-A010-10A-01W-A00E-09 g.chr15:42116162C>A c.4134C>A c.(4132-4134)ctC>ctA p.L1378L COADREAD 15 42116730 42116730 + Missense_Mutation SNP G G A TCGA-DM-A1D6-01A-21D-A152-10 TCGA-DM-A1D6-10A-01D-A152-10 g.chr15:42116730G>A c.4280G>A c.(4279-4281)cGc>cAc p.R1427H ESCA 15 42105843 42105843 + Missense_Mutation SNP G G A TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr15:42105843G>A c.862G>A c.(862-864)Gtg>Atg p.V288M ESCA 15 42106776 42106776 + Missense_Mutation SNP A A G TCGA-LN-A7HX-01A-11D-A33E-09 TCGA-LN-A7HX-10A-01D-A33H-09 g.chr15:42106776A>G c.1027A>G c.(1027-1029)Agg>Ggg p.R343G ESCA 15 42114464 42114464 + Missense_Mutation SNP T T C TCGA-LN-A7HV-01A-21D-A351-09 TCGA-LN-A7HV-10A-01D-A351-09 g.chr15:42114464T>C c.3091T>C c.(3091-3093)Tca>Cca p.S1031P ESCA 15 42115240 42115240 + Nonsense_Mutation SNP G G T TCGA-L5-A4OI-01A-11D-A27G-09 TCGA-L5-A4OI-11A-11D-A27G-09 g.chr15:42115240G>T c.3436G>T c.(3436-3438)Gga>Tga p.G1146* ESCA 15 42116141 42116141 + Missense_Mutation SNP G G T TCGA-IG-A51D-01A-11D-A27G-09 TCGA-IG-A51D-10A-01D-A27G-09 g.chr15:42116141G>T c.4113G>T c.(4111-4113)caG>caT p.Q1371H ESCA 15 42116219 42116219 + Missense_Mutation SNP G G T TCGA-L5-A8NH-01A-11D-A37C-09 TCGA-L5-A8NH-11A-11D-A37F-09 g.chr15:42116219G>T c.4191G>T c.(4189-4191)atG>atT p.M1397I GBM 15 42067489 42067489 + Missense_Mutation SNP T T G TCGA-28-2509-01A-01D-1494-08 TCGA-28-2509-10A-01D-1494-08 g.chr15:42067489T>G c.16T>G c.(16-18)Tca>Gca p.S6A GBM 15 42106769 42106769 + Silent SNP G G A TCGA-06-2563-01A-01D-1494-08 TCGA-06-2563-10A-01D-1494-08 g.chr15:42106769G>A c.1020G>A c.(1018-1020)gcG>gcA p.A340A GBM 15 42107465 42107465 + Silent SNP C C T TCGA-06-5856-01A-01D-1696-08 TCGA-06-5856-10A-01D-1696-08 g.chr15:42107465C>T c.1197C>T c.(1195-1197)ccC>ccT p.P399P GBM 15 42109162 42109162 + Missense_Mutation SNP C C T TCGA-16-0861-01A-01W-0424-08 TCGA-16-0861-10A-01W-0424-08 g.chr15:42109162C>T c.1658C>T c.(1657-1659)gCc>gTc p.A553V GBM 15 42111074 42111074 + Missense_Mutation SNP G G A TCGA-06-2563-01A-01D-1494-08 TCGA-06-2563-10A-01D-1494-08 g.chr15:42111074G>A c.2228G>A c.(2227-2229)cGt>cAt p.R743H GBM 15 42111153 42111153 + Silent SNP C C T TCGA-06-0174-01A-01D-1491-08 TCGA-06-0174-10B-01D-1491-08 g.chr15:42111153C>T c.2307C>T c.(2305-2307)aaC>aaT p.N769N GBMLGG 15 42067489 42067489 + Missense_Mutation SNP T T G TCGA-28-2509-01A-01D-1494-08 TCGA-28-2509-10A-01D-1494-08 g.chr15:42067489T>G c.16T>G c.(16-18)Tca>Gca p.S6A GBMLGG 15 42106769 42106769 + Silent SNP G G A TCGA-06-2563-01A-01D-1494-08 TCGA-06-2563-10A-01D-1494-08 g.chr15:42106769G>A c.1020G>A c.(1018-1020)gcG>gcA p.A340A GBMLGG 15 42107465 42107465 + Silent SNP C C T TCGA-06-5856-01A-01D-1696-08 TCGA-06-5856-10A-01D-1696-08 g.chr15:42107465C>T c.1197C>T c.(1195-1197)ccC>ccT p.P399P GBMLGG 15 42107938 42107938 + Silent SNP G G A TCGA-RY-A83Y-01A-11D-A36O-08 TCGA-RY-A83Y-10A-01D-A367-08 g.chr15:42107938G>A c.1452G>A c.(1450-1452)tcG>tcA p.S484S GBMLGG 15 42109134 42109134 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42109134C>T c.1630C>T c.(1630-1632)Cgg>Tgg p.R544W GBMLGG 15 42109162 42109162 + Missense_Mutation SNP C C T TCGA-16-0861-01A-01W-0424-08 TCGA-16-0861-10A-01W-0424-08 g.chr15:42109162C>T c.1658C>T c.(1657-1659)gCc>gTc p.A553V GBMLGG 15 42111074 42111074 + Missense_Mutation SNP G G A TCGA-06-2563-01A-01D-1494-08 TCGA-06-2563-10A-01D-1494-08 g.chr15:42111074G>A c.2228G>A c.(2227-2229)cGt>cAt p.R743H GBMLGG 15 42111153 42111153 + Silent SNP C C T TCGA-06-0174-01A-01D-1491-08 TCGA-06-0174-10B-01D-1491-08 g.chr15:42111153C>T c.2307C>T c.(2305-2307)aaC>aaT p.N769N GBMLGG 15 42113212 42113212 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42113212A>G c.2682A>G c.(2680-2682)ccA>ccG p.P894P HNSC 15 42067523 42067523 + Missense_Mutation SNP G G A TCGA-CR-7394-01A-11D-2012-08 TCGA-CR-7394-10A-01D-2013-08 g.chr15:42067523G>A c.50G>A c.(49-51)aGa>aAa p.R17K HNSC 15 42104154 42104154 + Splice_Site SNP G G A TCGA-CN-5369-01A-01D-1434-08 TCGA-CN-5369-10A-01D-1434-08 g.chr15:42104154G>A c.e6-1 HNSC 15 42107539 42107539 + Missense_Mutation SNP G G A TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:42107539G>A c.1271G>A c.(1270-1272)cGc>cAc p.R424H HNSC 15 42107957 42107957 + Missense_Mutation SNP G G C TCGA-CV-7250-01A-11D-2012-08 TCGA-CV-7250-10A-01D-2013-08 g.chr15:42107957G>C c.1471G>C c.(1471-1473)Gga>Cga p.G491R HNSC 15 42109197 42109197 + Missense_Mutation SNP G G A TCGA-CR-5248-01A-01D-2012-08 TCGA-CR-5248-10A-01D-2013-08 g.chr15:42109197G>A c.1693G>A c.(1693-1695)Gaa>Aaa p.E565K HNSC 15 42109605 42109605 + Silent SNP C C T TCGA-CV-7183-01A-11D-2012-08 TCGA-CV-7183-10A-01D-2013-08 g.chr15:42109605C>T c.1749C>T c.(1747-1749)cgC>cgT p.R583R HNSC 15 42110227 42110227 + Missense_Mutation SNP G G C TCGA-CR-6481-01A-11D-1870-08 TCGA-CR-6481-10A-01D-1870-08 g.chr15:42110227G>C c.1943G>C c.(1942-1944)gGa>gCa p.G648A HNSC 15 42110413 42110413 + Missense_Mutation SNP A A T TCGA-CV-5976-01A-11D-1683-08 TCGA-CV-5976-11A-01D-1683-08 g.chr15:42110413A>T c.2020A>T c.(2020-2022)Atc>Ttc p.I674F HNSC 15 42111558 42111558 + Silent SNP G G A TCGA-CR-7385-01A-11D-2012-08 TCGA-CR-7385-10A-01D-2013-08 g.chr15:42111558G>A c.2424G>A c.(2422-2424)aaG>aaA p.K808K HNSC 15 42113097 42113097 + Missense_Mutation SNP G G A TCGA-BA-5149-01A-01D-1512-08 TCGA-BA-5149-10A-01D-1512-08 g.chr15:42113097G>A c.2567G>A c.(2566-2568)cGc>cAc p.R856H HNSC 15 42113133 42113133 + Missense_Mutation SNP C C T TCGA-CR-7364-01A-11D-2012-08 TCGA-CR-7364-10A-01D-2013-08 g.chr15:42113133C>T c.2603C>T c.(2602-2604)tCc>tTc p.S868F HNSC 15 42113858 42113858 + Missense_Mutation SNP A A G TCGA-F7-A624-01A-22D-A30E-08 TCGA-F7-A624-10A-01D-A30H-08 g.chr15:42113858A>G c.2813A>G c.(2812-2814)gAa>gGa p.E938G HNSC 15 42113896 42113896 + Missense_Mutation SNP G G A TCGA-CN-A6V1-01A-12D-A34J-08 TCGA-CN-A6V1-10B-01D-A34M-08 g.chr15:42113896G>A c.2851G>A c.(2851-2853)Gaa>Aaa p.E951K HNSC 15 42114547 42114547 + Silent SNP C C A TCGA-CV-A6JO-01B-11D-A34J-08 TCGA-CV-A6JO-10A-01D-A34M-08 g.chr15:42114547C>A c.3174C>A c.(3172-3174)ggC>ggA p.G1058G HNSC 15 42115756 42115756 + Missense_Mutation SNP G G A TCGA-CV-6938-01A-11D-1912-08 TCGA-CV-6938-10A-01D-1912-08 g.chr15:42115756G>A c.3728G>A c.(3727-3729)cGg>cAg p.R1243Q HNSC 15 42116199 42116199 + Missense_Mutation SNP G G A TCGA-BB-A5HU-01A-11D-A28R-08 TCGA-BB-A5HU-10A-01D-A28U-08 g.chr15:42116199G>A c.4171G>A c.(4171-4173)Gag>Aag p.E1391K HNSC 15 42116702 42116702 + Nonsense_Mutation SNP C C T TCGA-CN-4740-01A-01D-1434-08 TCGA-CN-4740-10A-01D-1434-08 g.chr15:42116702C>T c.4252C>T c.(4252-4254)Cag>Tag p.Q1418* HNSC 15 42117604 42117604 + Silent SNP C C T TCGA-CR-7370-01A-11D-2129-08 TCGA-CR-7370-10A-01D-2129-08 g.chr15:42117604C>T c.4515C>T c.(4513-4515)gcC>gcT p.A1505A HNSC 15 42117612 42117612 + Missense_Mutation SNP G G A TCGA-HD-A633-01A-11D-A28R-08 TCGA-HD-A633-10A-01D-A28U-08 g.chr15:42117612G>A c.4523G>A c.(4522-4524)cGg>cAg p.R1508Q KICH 15 42113229 42113229 + Missense_Mutation SNP A A C TCGA-KL-8346-01A-11D-2310-10 TCGA-KL-8346-11A-01D-2310-10 g.chr15:42113229A>C c.2699A>C c.(2698-2700)cAt>cCt p.H900P KIPAN 15 42105966 42105966 + Missense_Mutation SNP G G A TCGA-BQ-5876-01A-11D-1589-08 TCGA-BQ-5876-11A-01D-1589-08 g.chr15:42105966G>A c.985G>A c.(985-987)Gtc>Atc p.V329I KIPAN 15 42107832 42107839 + Frame_Shift_Del DEL AAATCATC AAATCATC - TCGA-UZ-A9PL-01A-11D-A382-10 TCGA-UZ-A9PL-10A-01D-A385-10 g.chr15:42107832_42107839delAAATCATC c.1346_1353delAAATCATC c.(1345-1353)aaaatcatcfs p.KII449fs KIPAN 15 42107967 42107967 + Missense_Mutation SNP T T A TCGA-B2-3924-01A-02D-1386-10 TCGA-B2-3924-11A-01D-1251-10 g.chr15:42107967T>A c.1481T>A c.(1480-1482)cTa>cAa p.L494Q KIPAN 15 42108803 42108803 + Missense_Mutation SNP C C A TCGA-BP-5177-01A-01D-1429-08 TCGA-BP-5177-11A-01D-1429-08 g.chr15:42108803C>A c.1558C>A c.(1558-1560)Cat>Aat p.H520N KIPAN 15 42109123 42109123 + Missense_Mutation SNP C C A TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr15:42109123C>A c.1619C>A c.(1618-1620)gCa>gAa p.A540E KIPAN 15 42111022 42111022 + Splice_Site SNP T T C TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr15:42111022T>C c.2176T>C c.(2176-2178)Tgc>Cgc p.C726R KIPAN 15 42113229 42113229 + Missense_Mutation SNP A A C TCGA-KL-8346-01A-11D-2310-10 TCGA-KL-8346-11A-01D-2310-10 g.chr15:42113229A>C c.2699A>C c.(2698-2700)cAt>cCt p.H900P KIPAN 15 42113793 42113793 + Silent SNP C C A TCGA-B4-5844-01A-11D-1669-08 TCGA-B4-5844-10A-01D-1669-08 g.chr15:42113793C>A c.2748C>A c.(2746-2748)ccC>ccA p.P916P KIPAN 15 42114511 42114511 + Silent SNP G G A TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chr15:42114511G>A c.3138G>A c.(3136-3138)gaG>gaA p.E1046E KIRC 15 42107967 42107967 + Missense_Mutation SNP T T A TCGA-B2-3924-01A-02D-1386-10 TCGA-B2-3924-11A-01D-1251-10 g.chr15:42107967T>A c.1481T>A c.(1480-1482)cTa>cAa p.L494Q KIRC 15 42108803 42108803 + Missense_Mutation SNP C C A TCGA-BP-5177-01A-01D-1429-08 TCGA-BP-5177-11A-01D-1429-08 g.chr15:42108803C>A c.1558C>A c.(1558-1560)Cat>Aat p.H520N KIRC 15 42113793 42113793 + Silent SNP C C A TCGA-B4-5844-01A-11D-1669-08 TCGA-B4-5844-10A-01D-1669-08 g.chr15:42113793C>A c.2748C>A c.(2746-2748)ccC>ccA p.P916P KIRP 15 42105966 42105966 + Missense_Mutation SNP G G A TCGA-BQ-5876-01A-11D-1589-08 TCGA-BQ-5876-11A-01D-1589-08 g.chr15:42105966G>A c.985G>A c.(985-987)Gtc>Atc p.V329I KIRP 15 42107832 42107839 + Frame_Shift_Del DEL AAATCATC AAATCATC - TCGA-UZ-A9PL-01A-11D-A382-10 TCGA-UZ-A9PL-10A-01D-A385-10 g.chr15:42107832_42107839delAAATCATC c.1346_1353delAAATCATC c.(1345-1353)aaaatcatcfs p.KII449fs KIRP 15 42109123 42109123 + Missense_Mutation SNP C C A TCGA-SX-A7SS-01A-11D-A35Z-10 TCGA-SX-A7SS-10A-01D-A35Z-10 g.chr15:42109123C>A c.1619C>A c.(1618-1620)gCa>gAa p.A540E KIRP 15 42111022 42111022 + Splice_Site SNP T T C TCGA-IA-A83W-01A-11D-A34Z-10 TCGA-IA-A83W-11A-11D-A34Z-10 g.chr15:42111022T>C c.2176T>C c.(2176-2178)Tgc>Cgc p.C726R KIRP 15 42114511 42114511 + Silent SNP G G A TCGA-4A-A93W-01A-11D-A36X-10 TCGA-4A-A93W-10A-01D-A370-10 g.chr15:42114511G>A c.3138G>A c.(3136-3138)gaG>gaA p.E1046E LAML 15 42104229 42104229 + Silent SNP G G A TCGA-AB-2830-03B-01W-0728-08 TCGA-AB-2830-11B-01W-0728-08 g.chr15:42104229G>A c.402G>A c.(400-402)aaG>aaA p.K134K LGG 15 42107938 42107938 + Silent SNP G G A TCGA-RY-A83Y-01A-11D-A36O-08 TCGA-RY-A83Y-10A-01D-A367-08 g.chr15:42107938G>A c.1452G>A c.(1450-1452)tcG>tcA p.S484S LGG 15 42109134 42109134 + Missense_Mutation SNP C C T TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42109134C>T c.1630C>T c.(1630-1632)Cgg>Tgg p.R544W LGG 15 42113212 42113212 + Silent SNP A A G TCGA-DU-6392-01A-11D-1705-08 TCGA-DU-6392-10A-01D-1705-08 g.chr15:42113212A>G c.2682A>G c.(2680-2682)ccA>ccG p.P894P LIHC 15 42092080 42092080 + Frame_Shift_Del DEL C C - TCGA-G3-A3CJ-01A-11D-A20W-10 TCGA-G3-A3CJ-10A-01D-A20W-10 g.chr15:42092080delC c.174delC c.(172-174)gacfs p.D58fs LIHC 15 42104835 42104835 + Missense_Mutation SNP A A G TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr15:42104835A>G c.620A>G c.(619-621)gAc>gGc p.D207G LIHC 15 42106909 42106909 + Missense_Mutation SNP A A G TCGA-DD-AAEA-01A-11D-A40R-10 TCGA-DD-AAEA-10A-01D-A40U-10 g.chr15:42106909A>G c.1160A>G c.(1159-1161)tAt>tGt p.Y387C LIHC 15 42107824 42107824 + Silent SNP C C T TCGA-ES-A2HT-01A-12D-A183-10 TCGA-ES-A2HT-11A-11D-A183-10 g.chr15:42107824C>T c.1338C>T c.(1336-1338)gaC>gaT p.D446D LIHC 15 42110257 42110257 + Frame_Shift_Del DEL A A - TCGA-CC-5260-01A-01D-A12Z-10 TCGA-CC-5260-10B-01D-A12Z-10 g.chr15:42110257delA c.1973delA c.(1972-1974)cagfs p.Q658fs LIHC 15 42115228 42115228 + Missense_Mutation SNP G G A TCGA-DD-A113-01A-11D-A12Z-10 TCGA-DD-A113-10A-01D-A12Z-10 g.chr15:42115228G>A c.3424G>A c.(3424-3426)Gcc>Acc p.A1142T LUAD 15 42092020 42092020 + Splice_Site SNP G G T TCGA-95-7562-01A-11D-2238-08 TCGA-95-7562-10B-01D-2238-08 g.chr15:42092020G>T c.e3-1 LUAD 15 42105173 42105173 + Missense_Mutation SNP C C A TCGA-44-8117-01A-11D-2238-08 TCGA-44-8117-10A-01D-2238-08 g.chr15:42105173C>A c.693C>A c.(691-693)aaC>aaA p.N231K LUAD 15 42105896 42105896 + Missense_Mutation SNP C C G TCGA-55-8204-01A-11D-2238-08 TCGA-55-8204-10A-01D-2238-08 g.chr15:42105896C>G c.915C>G c.(913-915)ttC>ttG p.F305L LUAD 15 42105978 42105978 + Splice_Site SNP A A T TCGA-50-6594-01A-11D-1753-08 TCGA-50-6594-11A-01D-1753-08 g.chr15:42105978A>T c.997A>T c.(997-999)Agt>Tgt p.S333C LUAD 15 42107526 42107526 + Missense_Mutation SNP G G T TCGA-44-6145-01A-11D-1753-08 TCGA-44-6145-10A-01D-1753-08 g.chr15:42107526G>T c.1258G>T c.(1258-1260)Gac>Tac p.D420Y LUAD 15 42108778 42108778 + Silent SNP G G A TCGA-55-8208-01A-11D-2238-08 TCGA-55-8208-10A-01D-2238-08 g.chr15:42108778G>A c.1533G>A c.(1531-1533)ctG>ctA p.L511L LUAD 15 42108784 42108784 + Missense_Mutation SNP G G C TCGA-64-1677-01A-01W-0928-08 TCGA-64-1677-10A-01W-0928-08 g.chr15:42108784G>C c.1539G>C c.(1537-1539)gaG>gaC p.E513D LUAD 15 42109166 42109166 + Silent SNP G G T TCGA-73-4662-01A-01D-1265-08 TCGA-73-4662-11A-01D-1265-08 g.chr15:42109166G>T c.1662G>T c.(1660-1662)ggG>ggT p.G554G LUAD 15 42113112 42113112 + Missense_Mutation SNP G G T TCGA-55-8506-01A-11D-2393-08 TCGA-55-8506-10A-01D-2393-08 g.chr15:42113112G>T c.2582G>T c.(2581-2583)gGt>gTt p.G861V LUAD 15 42114454 42114454 + Missense_Mutation SNP T T A TCGA-55-8510-01A-11D-2393-08 TCGA-55-8510-10A-01D-2393-08 g.chr15:42114454T>A c.3081T>A c.(3079-3081)gaT>gaA p.D1027E LUAD 15 42115799 42115799 + Missense_Mutation SNP G G C TCGA-86-7955-01A-11D-2184-08 TCGA-86-7955-10A-01D-2184-08 g.chr15:42115799G>C c.3771G>C c.(3769-3771)aaG>aaC p.K1257N LUSC 15 42106796 42106796 + Silent SNP C C T TCGA-66-2789-01A-01D-0983-08 TCGA-66-2789-11A-01D-0983-08 g.chr15:42106796C>T c.1047C>T c.(1045-1047)gcC>gcT p.A349A LUSC 15 42107463 42107464 + Missense_Mutation DNP CC CC TT TCGA-18-3409-01A-01D-0983-08 TCGA-18-3409-11A-01D-0983-08 g.chr15:42107463_42107464CC>TT c.1195_1196CC>TT c.(1195-1197)CCc>TTc p.P399F LUSC 15 42109934 42109934 + Splice_Site SNP G G T TCGA-22-1012-01A-01D-1521-08 TCGA-22-1012-11A-01D-1521-08 g.chr15:42109934G>T c.e17+1 OV 15 42107468 42107468 + Silent SNP G G A TCGA-29-2432-01A-01D-1526-09 TCGA-29-2432-10A-01D-1526-09 g.chr15:42107468G>A c.1200G>A c.(1198-1200)gaG>gaA p.E400E PAAD 15 42107871 42107871 + Missense_Mutation SNP A A G TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:42107871A>G c.1385A>G c.(1384-1386)gAc>gGc p.D462G PAAD 15 42109604 42109604 + Missense_Mutation SNP G G A TCGA-FB-AAPS-01A-12D-A397-08 TCGA-FB-AAPS-11A-11D-A39A-08 g.chr15:42109604G>A c.1748G>A c.(1747-1749)cGc>cAc p.R583H PAAD 15 42116132 42116132 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:42116132C>T c.4104C>T c.(4102-4104)ccC>ccT p.P1368P PAAD 15 42116688 42116688 + Missense_Mutation SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:42116688C>T c.4238C>T c.(4237-4239)gCg>gTg p.A1413V PAAD 15 42117590 42117590 + Silent SNP C C T TCGA-IB-7651-01A-11D-2154-08 TCGA-IB-7651-10A-01D-2154-08 g.chr15:42117590C>T c.4501C>T c.(4501-4503)Ctg>Ttg p.L1501L PRAD 15 42105829 42105829 + Missense_Mutation SNP C C A TCGA-EJ-7797-01A-11D-2260-08 TCGA-EJ-7797-10A-01D-2260-08 g.chr15:42105829C>A c.848C>A c.(847-849)gCc>gAc p.A283D PRAD 15 42111443 42111443 + Splice_Site SNP G G T TCGA-XK-AAIW-01A-11D-A41K-08 TCGA-XK-AAIW-10A-01D-A41N-08 g.chr15:42111443G>T c.e22-1 READ 15 42103107 42103107 + Missense_Mutation SNP G G A TCGA-AG-3727-01A-01W-0899-10 TCGA-AG-3727-10A-01W-0901-10 g.chr15:42103107G>A c.233G>A c.(232-234)cGg>cAg p.R78Q READ 15 42106934 42106934 + Frame_Shift_Del DEL G G - TCGA-AG-4008-01A-01W-1073-09 TCGA-AG-4008-10A-01W-1073-09 g.chr15:42106934delG c.1185delG c.(1183-1185)gtgfs p.V395fs READ 15 42107532 42107532 + Missense_Mutation SNP A A G TCGA-EI-6507-01A-11D-1733-10 TCGA-EI-6507-10A-01D-1733-10 g.chr15:42107532A>G c.1264A>G c.(1264-1266)Acc>Gcc p.T422A SARC 15 42092030 42092030 + Missense_Mutation SNP G G A TCGA-DX-A8BP-01A-11D-A37C-09 TCGA-DX-A8BP-10A-01D-A37F-09 g.chr15:42092030G>A c.124G>A c.(124-126)Gag>Aag p.E42K SARC 15 42106769 42106769 + Silent SNP G G A TCGA-DX-A8BV-01A-11D-A37C-09 TCGA-DX-A8BV-10A-01D-A37F-09 g.chr15:42106769G>A c.1020G>A c.(1018-1020)gcG>gcA p.A340A SKCM 15 42067532 42067532 + Missense_Mutation SNP C C T TCGA-GN-A266-06A-11D-A197-08 TCGA-GN-A266-10A-01D-A199-08 g.chr15:42067532C>T c.59C>T c.(58-60)tCc>tTc p.S20F SKCM 15 42103103 42103103 + Missense_Mutation SNP C C T TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr15:42103103C>T c.229C>T c.(229-231)Ccc>Tcc p.P77S SKCM 15 42103104 42103104 + Missense_Mutation SNP C C T TCGA-DA-A1HY-06A-11D-A19A-08 TCGA-DA-A1HY-10A-01D-A19A-08 g.chr15:42103104C>T c.230C>T c.(229-231)cCc>cTc p.P77L SKCM 15 42104844 42104844 + Missense_Mutation SNP C C T TCGA-EE-A2MP-06A-11D-A197-08 TCGA-EE-A2MP-10A-01D-A199-08 g.chr15:42104844C>T c.629C>T c.(628-630)aCc>aTc p.T210I SKCM 15 42105143 42105143 + Silent SNP C C T TCGA-GF-A6C9-06A-11D-A30X-08 TCGA-GF-A6C9-10A-01D-A30X-08 g.chr15:42105143C>T c.663C>T c.(661-663)ggC>ggT p.G221G SKCM 15 42105202 42105202 + Missense_Mutation SNP G G A TCGA-D3-A5GU-06A-11D-A27K-08 TCGA-D3-A5GU-10A-01D-A27N-08 g.chr15:42105202G>A c.722G>A c.(721-723)aGa>aAa p.R241K SKCM 15 42105899 42105899 + Missense_Mutation SNP C C G TCGA-ER-A42K-06A-11D-A24R-08 TCGA-ER-A42K-10A-01D-A24R-08 g.chr15:42105899C>G c.918C>G c.(916-918)aaC>aaG p.N306K SKCM 15 42107506 42107506 + Missense_Mutation SNP C C T TCGA-D3-A51G-06A-11D-A25O-08 TCGA-D3-A51G-10A-01D-A25O-08 g.chr15:42107506C>T c.1238C>T c.(1237-1239)tCc>tTc p.S413F SKCM 15 42107506 42107506 + Missense_Mutation SNP C C T TCGA-EE-A3JA-06A-11D-A20D-08 TCGA-EE-A3JA-10A-01D-A20D-08 g.chr15:42107506C>T c.1238C>T c.(1237-1239)tCc>tTc p.S413F SKCM 15 42107533 42107533 + Missense_Mutation SNP C C T TCGA-RP-A695-06A-11D-A30X-08 TCGA-RP-A695-10A-01D-A30X-08 g.chr15:42107533C>T c.1265C>T c.(1264-1266)aCc>aTc p.T422I SKCM 15 42107932 42107932 + Silent SNP C C T TCGA-ER-A19F-06A-11D-A196-08 TCGA-ER-A19F-10A-01D-A198-08 g.chr15:42107932C>T c.1446C>T c.(1444-1446)atC>atT p.I482I SKCM 15 42109904 42109904 + Silent SNP G G A TCGA-EB-A5UN-06A-11D-A30X-08 TCGA-EB-A5UN-10A-01D-A30X-08 g.chr15:42109904G>A c.1893G>A c.(1891-1893)acG>acA p.T631T SKCM 15 42109932 42109932 + Splice_Site SNP C C T TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr15:42109932C>T c.1921C>T c.(1921-1923)Cgg>Tgg p.R641W SKCM 15 42110405 42110405 + Missense_Mutation SNP C C T TCGA-ER-A3PL-06A-11D-A23B-08 TCGA-ER-A3PL-10A-01D-A23B-08 g.chr15:42110405C>T c.2012C>T c.(2011-2013)cCc>cTc p.P671L SKCM 15 42111090 42111090 + Silent SNP C C T TCGA-FS-A1ZF-06A-12D-A197-08 TCGA-FS-A1ZF-10A-01D-A199-08 g.chr15:42111090C>T c.2244C>T c.(2242-2244)cgC>cgT p.R748R SKCM 15 42111098 42111098 + Missense_Mutation SNP A A G TCGA-D9-A6EC-06A-11D-A30X-08 TCGA-D9-A6EC-10A-01D-A30X-08 g.chr15:42111098A>G c.2252A>G c.(2251-2253)cAg>cGg p.Q751R SKCM 15 42111801 42111801 + Missense_Mutation SNP C C T TCGA-EE-A29E-06A-11D-A197-08 TCGA-EE-A29E-10A-01D-A199-08 g.chr15:42111801C>T c.2452C>T c.(2452-2454)Ccc>Tcc p.P818S SKCM 15 42113041 42113041 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:42113041C>T c.2511C>T c.(2509-2511)tcC>tcT p.S837S SKCM 15 42113243 42113243 + Missense_Mutation SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:42113243C>T c.2713C>T c.(2713-2715)Ctt>Ttt p.L905F SKCM 15 42113890 42113890 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:42113890C>T c.2845C>T c.(2845-2847)Ccc>Tcc p.P949S SKCM 15 42114441 42114441 + Missense_Mutation SNP C C T TCGA-EE-A29M-06A-11D-A196-08 TCGA-EE-A29M-10A-01D-A198-08 g.chr15:42114441C>T c.3068C>T c.(3067-3069)cCc>cTc p.P1023L SKCM 15 42115750 42115750 + Missense_Mutation SNP C C T TCGA-GN-A262-06A-11D-A196-08 TCGA-GN-A262-10A-01D-A198-08 g.chr15:42115750C>T c.3722C>T c.(3721-3723)cCg>cTg p.P1241L SKCM 15 42116018 42116018 + Silent SNP C C T TCGA-FW-A3R5-06A-11D-A23B-08 TCGA-FW-A3R5-10A-01D-A23B-08 g.chr15:42116018C>T c.3990C>T c.(3988-3990)ttC>ttT p.F1330F SKCM 15 42116019 42116019 + Missense_Mutation SNP C C T TCGA-EE-A3J7-06A-11D-A20D-08 TCGA-EE-A3J7-10A-01D-A20D-08 g.chr15:42116019C>T c.3991C>T c.(3991-3993)Ccg>Tcg p.P1331S SKCM 15 42116122 42116122 + Missense_Mutation SNP C C T TCGA-D3-A51E-06A-11D-A25O-08 TCGA-D3-A51E-10A-01D-A25O-08 g.chr15:42116122C>T c.4094C>T c.(4093-4095)cCc>cTc p.P1365L SKCM 15 42117477 42117477 + Missense_Mutation SNP C C T TCGA-FS-A1ZA-06A-11D-A197-08 TCGA-FS-A1ZA-10A-01D-A199-08 g.chr15:42117477C>T c.4388C>T c.(4387-4389)tCa>tTa p.S1463L

Mutation - ICGC Project Code Chromosome Chromosome Start Chromosome End Mutation Type Mutated from Allele Mutated to Allele Consequence Type AA Mutation CDS Mutation BLCA-US 15 42092064 42092064 single base substitution G T exon_variant BLCA-US 15 42092064 42092064 single base substitution G T intron_variant BLCA-US 15 42092064 42092064 single base substitution G T missense_variant R53I 158G>T BLCA-US 15 42092078 42092078 single base substitution G A exon_variant BLCA-US 15 42092078 42092078 single base substitution G A intron_variant BLCA-US 15 42092078 42092078 single base substitution G A missense_variant D58N 172G>A BLCA-US 15 42107900 42107900 single base substitution G A 3_prime_UTR_variant BLCA-US 15 42107900 42107900 single base substitution G A downstream_gene_variant BLCA-US 15 42107900 42107900 single base substitution G A exon_variant BLCA-US 15 42107900 42107900 single base substitution G A missense_variant D305N 913G>A BLCA-US 15 42107900 42107900 single base substitution G A missense_variant D349N 1045G>A BLCA-US 15 42107900 42107900 single base substitution G A missense_variant D466N 1396G>A BLCA-US 15 42107900 42107900 single base substitution G A missense_variant D472N 1414G>A BLCA-US 15 42107900 42107900 single base substitution G A upstream_gene_variant BLCA-US 15 42113042 42113042 single base substitution G A 3_prime_UTR_variant BLCA-US 15 42113042 42113042 single base substitution G A downstream_gene_variant BLCA-US 15 42113042 42113042 single base substitution G A exon_variant BLCA-US 15 42113042 42113042 single base substitution G A missense_variant V671M 2011G>A BLCA-US 15 42113042 42113042 single base substitution G A missense_variant V715M 2143G>A BLCA-US 15 42113042 42113042 single base substitution G A missense_variant V832M 2494G>A BLCA-US 15 42113042 42113042 single base substitution G A missense_variant V838M 2512G>A BLCA-US 15 42113042 42113042 single base substitution G A upstream_gene_variant BOCA-FR 15 42107358 42107358 single base substitution C T downstream_gene_variant BOCA-FR 15 42107358 42107358 single base substitution C T intron_variant BOCA-FR 15 42107358 42107358 single base substitution C T upstream_gene_variant BRCA-EU 15 42062060 42062060 single base substitution G T upstream_gene_variant BRCA-EU 15 42062965 42062965 single base substitution C T upstream_gene_variant BRCA-EU 15 42063078 42063078 single base substitution G T upstream_gene_variant BRCA-EU 15 42064430 42064430 deletion of <=200bp A - upstream_gene_variant BRCA-EU 15 42065648 42065648 single base substitution C G upstream_gene_variant BRCA-EU 15 42069454 42069454 single base substitution G A intron_variant BRCA-EU 15 42069493 42069493 single base substitution C T intron_variant BRCA-EU 15 42072276 42072276 single base substitution C T intron_variant BRCA-EU 15 42073254 42073254 insertion of <=200bp - T intron_variant BRCA-EU 15 42075790 42075790 single base substitution G A intron_variant BRCA-EU 15 42076686 42076686 single base substitution A T intron_variant BRCA-EU 15 42080317 42080317 single base substitution G A intron_variant BRCA-EU 15 42081849 42081849 single base substitution T C intron_variant BRCA-EU 15 42082529 42082529 single base substitution C G intron_variant BRCA-EU 15 42082836 42082836 deletion of <=200bp T - intron_variant BRCA-EU 15 42083744 42083744 single base substitution G A intron_variant BRCA-EU 15 42085586 42085586 single base substitution G A intron_variant BRCA-EU 15 42085719 42085719 single base substitution A G intron_variant BRCA-EU 15 42088399 42088399 single base substitution G T intron_variant BRCA-EU 15 42092686 42092686 single base substitution G A intron_variant BRCA-EU 15 42092778 42092778 single base substitution C A intron_variant BRCA-EU 15 42096428 42096428 single base substitution C A intron_variant BRCA-EU 15 42098384 42098384 single base substitution C G intron_variant BRCA-EU 15 42098384 42098384 single base substitution C G upstream_gene_variant BRCA-EU 15 42099606 42099606 single base substitution A T intron_variant BRCA-EU 15 42099606 42099606 single base substitution A T upstream_gene_variant BRCA-EU 15 42100138 42100138 single base substitution G A intron_variant BRCA-EU 15 42100138 42100138 single base substitution G A upstream_gene_variant BRCA-EU 15 42100415 42100415 single base substitution C T intron_variant BRCA-EU 15 42100415 42100415 single base substitution C T upstream_gene_variant BRCA-EU 15 42100461 42100461 single base substitution C T intron_variant BRCA-EU 15 42100461 42100461 single base substitution C T upstream_gene_variant BRCA-EU 15 42100599 42100599 single base substitution G A intron_variant BRCA-EU 15 42100599 42100599 single base substitution G A upstream_gene_variant BRCA-EU 15 42102631 42102631 single base substitution G A intron_variant BRCA-EU 15 42102631 42102631 single base substitution G A upstream_gene_variant BRCA-EU 15 42103226 42103226 single base substitution G A intron_variant BRCA-EU 15 42104111 42104111 single base substitution G T downstream_gene_variant BRCA-EU 15 42104111 42104111 single base substitution G T intron_variant BRCA-EU 15 42104111 42104111 single base substitution G T upstream_gene_variant BRCA-EU 15 42104419 42104419 insertion of <=200bp - C downstream_gene_variant BRCA-EU 15 42104419 42104419 insertion of <=200bp - C intron_variant BRCA-EU 15 42104419 42104419 insertion of <=200bp - C upstream_gene_variant BRCA-EU 15 42104588 42104588 single base substitution G T downstream_gene_variant BRCA-EU 15 42104588 42104588 single base substitution G T intron_variant BRCA-EU 15 42104588 42104588 single base substitution G T upstream_gene_variant BRCA-EU 15 42104946 42104946 single base substitution C T downstream_gene_variant BRCA-EU 15 42104946 42104946 single base substitution C T exon_variant BRCA-EU 15 42104946 42104946 single base substitution C T intron_variant BRCA-EU 15 42104946 42104946 single base substitution C T upstream_gene_variant BRCA-EU 15 42106749 42106749 single base substitution C T downstream_gene_variant BRCA-EU 15 42106749 42106749 single base substitution C T intron_variant BRCA-EU 15 42106749 42106749 single base substitution C T missense_variant R216C 646C>T BRCA-EU 15 42106749 42106749 single base substitution C T missense_variant R328C 982C>T BRCA-EU 15 42106749 42106749 single base substitution C T missense_variant R334C 1000C>T BRCA-EU 15 42106749 42106749 single base substitution C T splice_region_variant BRCA-EU 15 42106749 42106749 single base substitution C T upstream_gene_variant BRCA-EU 15 42113111 42113111 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 42113111 42113111 single base substitution G A downstream_gene_variant BRCA-EU 15 42113111 42113111 single base substitution G A exon_variant BRCA-EU 15 42113111 42113111 single base substitution G A missense_variant G694S 2080G>A BRCA-EU 15 42113111 42113111 single base substitution G A missense_variant G738S 2212G>A BRCA-EU 15 42113111 42113111 single base substitution G A missense_variant G855S 2563G>A BRCA-EU 15 42113111 42113111 single base substitution G A missense_variant G861S 2581G>A BRCA-EU 15 42113111 42113111 single base substitution G A upstream_gene_variant BRCA-EU 15 42115106 42115106 single base substitution C G downstream_gene_variant BRCA-EU 15 42115106 42115106 single base substitution C G exon_variant BRCA-EU 15 42115106 42115106 single base substitution C G intron_variant BRCA-EU 15 42116073 42116073 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 42116073 42116073 single base substitution G A downstream_gene_variant BRCA-EU 15 42116073 42116073 single base substitution G A exon_variant BRCA-EU 15 42116073 42116073 single base substitution G A intron_variant BRCA-EU 15 42116073 42116073 single base substitution G A missense_variant E1182K 3544G>A BRCA-EU 15 42116073 42116073 single base substitution G A missense_variant E1226K 3676G>A BRCA-EU 15 42116073 42116073 single base substitution G A missense_variant E1343K 4027G>A BRCA-EU 15 42116073 42116073 single base substitution G A missense_variant E1349K 4045G>A BRCA-EU 15 42116199 42116199 single base substitution G A 3_prime_UTR_variant BRCA-EU 15 42116199 42116199 single base substitution G A downstream_gene_variant BRCA-EU 15 42116199 42116199 single base substitution G A exon_variant BRCA-EU 15 42116199 42116199 single base substitution G A intron_variant BRCA-EU 15 42116199 42116199 single base substitution G A missense_variant E1224K 3670G>A BRCA-EU 15 42116199 42116199 single base substitution G A missense_variant E1268K 3802G>A BRCA-EU 15 42116199 42116199 single base substitution G A missense_variant E1385K 4153G>A BRCA-EU 15 42116199 42116199 single base substitution G A missense_variant E1391K 4171G>A BRCA-EU 15 42116306 42116306 single base substitution C G downstream_gene_variant BRCA-EU 15 42116306 42116306 single base substitution C G intron_variant BRCA-EU 15 42116799 42116799 deletion of <=200bp G - downstream_gene_variant BRCA-EU 15 42116799 42116799 deletion of <=200bp G - intron_variant BRCA-EU 15 42118922 42118922 single base substitution G C 3_prime_UTR_variant BRCA-EU 15 42118922 42118922 single base substitution G C downstream_gene_variant BRCA-EU 15 42120006 42120006 single base substitution C G 3_prime_UTR_variant BRCA-EU 15 42120006 42120006 single base substitution C G downstream_gene_variant BRCA-EU 15 42122359 42122359 single base substitution G C downstream_gene_variant BRCA-EU 15 42124373 42124373 single base substitution G A downstream_gene_variant BRCA-FR 15 42079222 42079222 single base substitution G A intron_variant BRCA-FR 15 42080317 42080317 single base substitution G A intron_variant BRCA-FR 15 42083744 42083744 single base substitution G A intron_variant BRCA-FR 15 42113111 42113111 single base substitution G A 3_prime_UTR_variant BRCA-FR 15 42113111 42113111 single base substitution G A downstream_gene_variant BRCA-FR 15 42113111 42113111 single base substitution G A exon_variant BRCA-FR 15 42113111 42113111 single base substitution G A missense_variant G694S 2080G>A BRCA-FR 15 42113111 42113111 single base substitution G A missense_variant G738S 2212G>A BRCA-FR 15 42113111 42113111 single base substitution G A missense_variant G855S 2563G>A BRCA-FR 15 42113111 42113111 single base substitution G A missense_variant G861S 2581G>A BRCA-FR 15 42113111 42113111 single base substitution G A upstream_gene_variant BRCA-FR 15 42116306 42116306 single base substitution C G downstream_gene_variant BRCA-FR 15 42116306 42116306 single base substitution C G intron_variant BRCA-FR 15 42124373 42124373 single base substitution G A downstream_gene_variant BRCA-KR 15 42115371 42115371 single base substitution C A 3_prime_UTR_variant BRCA-KR 15 42115371 42115371 single base substitution C A downstream_gene_variant BRCA-KR 15 42115371 42115371 single base substitution C A exon_variant BRCA-KR 15 42115371 42115371 single base substitution C A intron_variant BRCA-KR 15 42115371 42115371 single base substitution C A synonymous_variant P1022P 3066C>A BRCA-KR 15 42115371 42115371 single base substitution C A synonymous_variant P1066P 3198C>A BRCA-KR 15 42115371 42115371 single base substitution C A synonymous_variant P1183P 3549C>A BRCA-KR 15 42115371 42115371 single base substitution C A synonymous_variant P1189P 3567C>A BRCA-UK 15 42104588 42104588 single base substitution G T downstream_gene_variant BRCA-UK 15 42104588 42104588 single base substitution G T intron_variant BRCA-UK 15 42104588 42104588 single base substitution G T upstream_gene_variant BRCA-UK 15 42107841 42107841 single base substitution A G 3_prime_UTR_variant BRCA-UK 15 42107841 42107841 single base substitution A G downstream_gene_variant BRCA-UK 15 42107841 42107841 single base substitution A G exon_variant BRCA-UK 15 42107841 42107841 single base substitution A G missense_variant Y285C 854A>G BRCA-UK 15 42107841 42107841 single base substitution A G missense_variant Y329C 986A>G BRCA-UK 15 42107841 42107841 single base substitution A G missense_variant Y446C 1337A>G BRCA-UK 15 42107841 42107841 single base substitution A G missense_variant Y452C 1355A>G BRCA-UK 15 42107841 42107841 single base substitution A G upstream_gene_variant BRCA-UK 15 42113798 42113798 single base substitution G T 3_prime_UTR_variant BRCA-UK 15 42113798 42113798 single base substitution G T downstream_gene_variant BRCA-UK 15 42113798 42113798 single base substitution G T exon_variant BRCA-UK 15 42113798 42113798 single base substitution G T missense_variant R751L 2252G>T BRCA-UK 15 42113798 42113798 single base substitution G T missense_variant R795L 2384G>T BRCA-UK 15 42113798 42113798 single base substitution G T missense_variant R912L 2735G>T BRCA-UK 15 42113798 42113798 single base substitution G T missense_variant R918L 2753G>T BRCA-UK 15 42113798 42113798 single base substitution G T upstream_gene_variant BRCA-US 15 42104263 42104263 single base substitution G A 3_prime_UTR_variant BRCA-US 15 42104263 42104263 single base substitution G A downstream_gene_variant BRCA-US 15 42104263 42104263 single base substitution G A exon_variant BRCA-US 15 42104263 42104263 single base substitution G A missense_variant A146T 436G>A BRCA-US 15 42104263 42104263 single base substitution G A missense_variant A34T 100G>A BRCA-US 15 42104263 42104263 single base substitution G A upstream_gene_variant BRCA-US 15 42104774 42104774 single base substitution G A 3_prime_UTR_variant BRCA-US 15 42104774 42104774 single base substitution G A downstream_gene_variant BRCA-US 15 42104774 42104774 single base substitution G A exon_variant BRCA-US 15 42104774 42104774 single base substitution G A missense_variant E187K 559G>A BRCA-US 15 42104774 42104774 single base substitution G A missense_variant E75K 223G>A BRCA-US 15 42104774 42104774 single base substitution G A upstream_gene_variant BRCA-US 15 42110267 42110267 single base substitution C T 3_prime_UTR_variant BRCA-US 15 42110267 42110267 single base substitution C T downstream_gene_variant BRCA-US 15 42110267 42110267 single base substitution C T exon_variant BRCA-US 15 42110267 42110267 single base substitution C T synonymous_variant D494D 1482C>T BRCA-US 15 42110267 42110267 single base substitution C T synonymous_variant D538D 1614C>T BRCA-US 15 42110267 42110267 single base substitution C T synonymous_variant D655D 1965C>T BRCA-US 15 42110267 42110267 single base substitution C T synonymous_variant D661D 1983C>T BRCA-US 15 42110267 42110267 single base substitution C T upstream_gene_variant BRCA-US 15 42111445 42111445 single base substitution C T downstream_gene_variant BRCA-US 15 42111445 42111445 single base substitution C T missense_variant H604Y 1810C>T BRCA-US 15 42111445 42111445 single base substitution C T missense_variant H648Y 1942C>T BRCA-US 15 42111445 42111445 single base substitution C T missense_variant H765Y 2293C>T BRCA-US 15 42111445 42111445 single base substitution C T missense_variant H771Y 2311C>T BRCA-US 15 42111445 42111445 single base substitution C T splice_region_variant BRCA-US 15 42111445 42111445 single base substitution C T upstream_gene_variant BRCA-US 15 42113197 42113197 single base substitution G C 3_prime_UTR_variant BRCA-US 15 42113197 42113197 single base substitution G C downstream_gene_variant BRCA-US 15 42113197 42113197 single base substitution G C exon_variant BRCA-US 15 42113197 42113197 single base substitution G C synonymous_variant S722S 2166G>C BRCA-US 15 42113197 42113197 single base substitution G C synonymous_variant S766S 2298G>C BRCA-US 15 42113197 42113197 single base substitution G C synonymous_variant S883S 2649G>C BRCA-US 15 42113197 42113197 single base substitution G C synonymous_variant S889S 2667G>C BRCA-US 15 42113197 42113197 single base substitution G C upstream_gene_variant BRCA-US 15 42114459 42114459 single base substitution T C 3_prime_UTR_variant BRCA-US 15 42114459 42114459 single base substitution T C exon_variant BRCA-US 15 42114459 42114459 single base substitution T C missense_variant I1023T 3068T>C BRCA-US 15 42114459 42114459 single base substitution T C missense_variant I1029T 3086T>C BRCA-US 15 42114459 42114459 single base substitution T C missense_variant I862T 2585T>C BRCA-US 15 42114459 42114459 single base substitution T C missense_variant I906T 2717T>C BRCA-US 15 42114459 42114459 single base substitution T C upstream_gene_variant BRCA-US 15 42115323 42115323 single base substitution C G 3_prime_UTR_variant BRCA-US 15 42115323 42115323 single base substitution C G downstream_gene_variant BRCA-US 15 42115323 42115323 single base substitution C G exon_variant BRCA-US 15 42115323 42115323 single base substitution C G intron_variant BRCA-US 15 42115323 42115323 single base substitution C G synonymous_variant L1006L 3018C>G BRCA-US 15 42115323 42115323 single base substitution C G synonymous_variant L1050L 3150C>G BRCA-US 15 42115323 42115323 single base substitution C G synonymous_variant L1167L 3501C>G BRCA-US 15 42115323 42115323 single base substitution C G synonymous_variant L1173L 3519C>G BRCA-US 15 42115928 42115928 single base substitution C T 3_prime_UTR_variant BRCA-US 15 42115928 42115928 single base substitution C T downstream_gene_variant BRCA-US 15 42115928 42115928 single base substitution C T exon_variant BRCA-US 15 42115928 42115928 single base substitution C T intron_variant BRCA-US 15 42115928 42115928 single base substitution C T synonymous_variant I1133I 3399C>T BRCA-US 15 42115928 42115928 single base substitution C T synonymous_variant I1177I 3531C>T BRCA-US 15 42115928 42115928 single base substitution C T synonymous_variant I1294I 3882C>T BRCA-US 15 42115928 42115928 single base substitution C T synonymous_variant I1300I 3900C>T BRCA-US 15 42115998 42115998 single base substitution G A 3_prime_UTR_variant BRCA-US 15 42115998 42115998 single base substitution G A downstream_gene_variant BRCA-US 15 42115998 42115998 single base substitution G A exon_variant BRCA-US 15 42115998 42115998 single base substitution G A intron_variant BRCA-US 15 42115998 42115998 single base substitution G A missense_variant E1157K 3469G>A BRCA-US 15 42115998 42115998 single base substitution G A missense_variant E1201K 3601G>A BRCA-US 15 42115998 42115998 single base substitution G A missense_variant E1318K 3952G>A BRCA-US 15 42115998 42115998 single base substitution G A missense_variant E1324K 3970G>A BTCA-JP 15 42106750 42106750 single base substitution G A downstream_gene_variant BTCA-JP 15 42106750 42106750 single base substitution G A intron_variant BTCA-JP 15 42106750 42106750 single base substitution G A missense_variant R216H 647G>A BTCA-JP 15 42106750 42106750 single base substitution G A missense_variant R328H 983G>A BTCA-JP 15 42106750 42106750 single base substitution G A missense_variant R334H 1001G>A BTCA-JP 15 42106750 42106750 single base substitution G A splice_region_variant BTCA-JP 15 42106750 42106750 single base substitution G A upstream_gene_variant BTCA-JP 15 42109141 42109141 single base substitution G A 3_prime_UTR_variant BTCA-JP 15 42109141 42109141 single base substitution G A downstream_gene_variant BTCA-JP 15 42109141 42109141 single base substitution G A exon_variant BTCA-JP 15 42109141 42109141 single base substitution G A missense_variant R379Q 1136G>A BTCA-JP 15 42109141 42109141 single base substitution G A missense_variant R423Q 1268G>A BTCA-JP 15 42109141 42109141 single base substitution G A missense_variant R540Q 1619G>A BTCA-JP 15 42109141 42109141 single base substitution G A missense_variant R546Q 1637G>A BTCA-JP 15 42109141 42109141 single base substitution G A upstream_gene_variant BTCA-JP 15 42110316 42110316 single base substitution C T downstream_gene_variant BTCA-JP 15 42110316 42110316 single base substitution C T intron_variant BTCA-JP 15 42110316 42110316 single base substitution C T upstream_gene_variant BTCA-JP 15 42113984 42113984 single base substitution G A downstream_gene_variant BTCA-JP 15 42113984 42113984 single base substitution G A intron_variant BTCA-JP 15 42113984 42113984 single base substitution G A upstream_gene_variant BTCA-JP 15 42115176 42115176 single base substitution G A 3_prime_UTR_variant BTCA-JP 15 42115176 42115176 single base substitution G A downstream_gene_variant BTCA-JP 15 42115176 42115176 single base substitution G A exon_variant BTCA-JP 15 42115176 42115176 single base substitution G A synonymous_variant S1001S 3003G>A BTCA-JP 15 42115176 42115176 single base substitution G A synonymous_variant S1118S 3354G>A BTCA-JP 15 42115176 42115176 single base substitution G A synonymous_variant S1124S 3372G>A BTCA-JP 15 42115176 42115176 single base substitution G A synonymous_variant S957S 2871G>A CESC-US 15 42067565 42067565 single base substitution G A 5_prime_UTR_variant CESC-US 15 42067565 42067565 single base substitution G A exon_variant CESC-US 15 42067565 42067565 single base substitution G A missense_variant R31Q 92G>A CESC-US 15 42107876 42107876 single base substitution G C 3_prime_UTR_variant CESC-US 15 42107876 42107876 single base substitution G C downstream_gene_variant CESC-US 15 42107876 42107876 single base substitution G C exon_variant CESC-US 15 42107876 42107876 single base substitution G C missense_variant E297Q 889G>C CESC-US 15 42107876 42107876 single base substitution G C missense_variant E341Q 1021G>C CESC-US 15 42107876 42107876 single base substitution G C missense_variant E458Q 1372G>C CESC-US 15 42107876 42107876 single base substitution G C missense_variant E464Q 1390G>C CESC-US 15 42107876 42107876 single base substitution G C upstream_gene_variant CESC-US 15 42116052 42116052 single base substitution G T 3_prime_UTR_variant CESC-US 15 42116052 42116052 single base substitution G T downstream_gene_variant CESC-US 15 42116052 42116052 single base substitution G T exon_variant CESC-US 15 42116052 42116052 single base substitution G T intron_variant CESC-US 15 42116052 42116052 single base substitution G T stop_gained E1175* 3523G>T CESC-US 15 42116052 42116052 single base substitution G T stop_gained E1219* 3655G>T CESC-US 15 42116052 42116052 single base substitution G T stop_gained E1336* 4006G>T CESC-US 15 42116052 42116052 single base substitution G T stop_gained E1342* 4024G>T CLLE-ES 15 42073572 42073572 single base substitution G C intron_variant CLLE-ES 15 42082081 42082081 single base substitution T C intron_variant CLLE-ES 15 42091840 42091840 single base substitution C T intron_variant COAD-US 15 42104313 42104313 single base substitution G A 3_prime_UTR_variant COAD-US 15 42104313 42104313 single base substitution G A downstream_gene_variant COAD-US 15 42104313 42104313 single base substitution G A exon_variant COAD-US 15 42104313 42104313 single base substitution G A synonymous_variant V162V 486G>A COAD-US 15 42104313 42104313 single base substitution G A synonymous_variant V50V 150G>A COAD-US 15 42104313 42104313 single base substitution G A upstream_gene_variant COAD-US 15 42105244 42105244 single base substitution G T 3_prime_UTR_variant COAD-US 15 42105244 42105244 single base substitution G T downstream_gene_variant COAD-US 15 42105244 42105244 single base substitution G T exon_variant COAD-US 15 42105244 42105244 single base substitution G T missense_variant G143V 428G>T COAD-US 15 42105244 42105244 single base substitution G T missense_variant G255V 764G>T COAD-US 15 42105244 42105244 single base substitution G T upstream_gene_variant COAD-US 15 42110446 42110446 single base substitution C A 3_prime_UTR_variant COAD-US 15 42110446 42110446 single base substitution C A downstream_gene_variant COAD-US 15 42110446 42110446 single base substitution C A exon_variant COAD-US 15 42110446 42110446 single base substitution C A missense_variant L518I 1552C>A COAD-US 15 42110446 42110446 single base substitution C A missense_variant L562I 1684C>A COAD-US 15 42110446 42110446 single base substitution C A missense_variant L679I 2035C>A COAD-US 15 42110446 42110446 single base substitution C A missense_variant L685I 2053C>A COAD-US 15 42110446 42110446 single base substitution C A upstream_gene_variant COAD-US 15 42113931 42113931 single base substitution C T 3_prime_UTR_variant COAD-US 15 42113931 42113931 single base substitution C T downstream_gene_variant COAD-US 15 42113931 42113931 single base substitution C T exon_variant COAD-US 15 42113931 42113931 single base substitution C T synonymous_variant N795N 2385C>T COAD-US 15 42113931 42113931 single base substitution C T synonymous_variant N839N 2517C>T COAD-US 15 42113931 42113931 single base substitution C T synonymous_variant N956N 2868C>T COAD-US 15 42113931 42113931 single base substitution C T synonymous_variant N962N 2886C>T COAD-US 15 42113931 42113931 single base substitution C T upstream_gene_variant COAD-US 15 42115703 42115703 single base substitution C T 3_prime_UTR_variant COAD-US 15 42115703 42115703 single base substitution C T downstream_gene_variant COAD-US 15 42115703 42115703 single base substitution C T exon_variant COAD-US 15 42115703 42115703 single base substitution C T intron_variant COAD-US 15 42115703 42115703 single base substitution C T synonymous_variant I1058I 3174C>T COAD-US 15 42115703 42115703 single base substitution C T synonymous_variant I1102I 3306C>T COAD-US 15 42115703 42115703 single base substitution C T synonymous_variant I1219I 3657C>T COAD-US 15 42115703 42115703 single base substitution C T synonymous_variant I1225I 3675C>T COAD-US 15 42116730 42116730 single base substitution G A 3_prime_UTR_variant COAD-US 15 42116730 42116730 single base substitution G A downstream_gene_variant COAD-US 15 42116730 42116730 single base substitution G A exon_variant COAD-US 15 42116730 42116730 single base substitution G A missense_variant R1144H 3431G>A COAD-US 15 42116730 42116730 single base substitution G A missense_variant R1260H 3779G>A COAD-US 15 42116730 42116730 single base substitution G A missense_variant R1304H 3911G>A COAD-US 15 42116730 42116730 single base substitution G A missense_variant R1421H 4262G>A COAD-US 15 42116730 42116730 single base substitution G A missense_variant R1427H 4280G>A COAD-US 15 42117615 42117615 single base substitution G A 3_prime_UTR_variant COAD-US 15 42117615 42117615 single base substitution G A downstream_gene_variant COAD-US 15 42117615 42117615 single base substitution G A exon_variant COAD-US 15 42117615 42117615 single base substitution G A missense_variant R1226H 3677G>A COAD-US 15 42117615 42117615 single base substitution G A missense_variant R1342H 4025G>A COAD-US 15 42117615 42117615 single base substitution G A missense_variant R1386H 4157G>A COAD-US 15 42117615 42117615 single base substitution G A missense_variant R1503H 4508G>A COAD-US 15 42117615 42117615 single base substitution G A missense_variant R1509H 4526G>A COAD-US 15 42120375 42120375 single base substitution C T downstream_gene_variant COCA-CN 15 42103500 42103500 single base substitution C T exon_variant COCA-CN 15 42103500 42103500 single base substitution C T intron_variant COCA-CN 15 42103500 42103500 single base substitution C T upstream_gene_variant COCA-CN 15 42104637 42104637 single base substitution C A downstream_gene_variant COCA-CN 15 42104637 42104637 single base substitution C A intron_variant COCA-CN 15 42104637 42104637 single base substitution C A upstream_gene_variant COCA-CN 15 42107482 42107482 single base substitution A G 3_prime_UTR_variant COCA-CN 15 42107482 42107482 single base substitution A G downstream_gene_variant COCA-CN 15 42107482 42107482 single base substitution A G exon_variant COCA-CN 15 42107482 42107482 single base substitution A G intron_variant COCA-CN 15 42107482 42107482 single base substitution A G missense_variant N282S 845A>G COCA-CN 15 42107482 42107482 single base substitution A G missense_variant N399S 1196A>G COCA-CN 15 42107482 42107482 single base substitution A G missense_variant N405S 1214A>G COCA-CN 15 42107482 42107482 single base substitution A G upstream_gene_variant COCA-CN 15 42107539 42107539 single base substitution G A 3_prime_UTR_variant COCA-CN 15 42107539 42107539 single base substitution G A downstream_gene_variant COCA-CN 15 42107539 42107539 single base substitution G A exon_variant COCA-CN 15 42107539 42107539 single base substitution G A intron_variant COCA-CN 15 42107539 42107539 single base substitution G A missense_variant R301H 902G>A COCA-CN 15 42107539 42107539 single base substitution G A missense_variant R418H 1253G>A COCA-CN 15 42107539 42107539 single base substitution G A missense_variant R424H 1271G>A COCA-CN 15 42107539 42107539 single base substitution G A upstream_gene_variant COCA-CN 15 42109713 42109713 single base substitution T C downstream_gene_variant COCA-CN 15 42109713 42109713 single base substitution T C intron_variant COCA-CN 15 42109713 42109713 single base substitution T C upstream_gene_variant COCA-CN 15 42110526 42110526 insertion of <=200bp - T downstream_gene_variant COCA-CN 15 42110526 42110526 insertion of <=200bp - T intron_variant COCA-CN 15 42110526 42110526 insertion of <=200bp - T upstream_gene_variant COCA-CN 15 42111037 42111037 single base substitution C T 3_prime_UTR_variant COCA-CN 15 42111037 42111037 single base substitution C T downstream_gene_variant COCA-CN 15 42111037 42111037 single base substitution C T exon_variant COCA-CN 15 42111037 42111037 single base substitution C T missense_variant R564C 1690C>T COCA-CN 15 42111037 42111037 single base substitution C T missense_variant R608C 1822C>T COCA-CN 15 42111037 42111037 single base substitution C T missense_variant R725C 2173C>T COCA-CN 15 42111037 42111037 single base substitution C T missense_variant R731C 2191C>T COCA-CN 15 42111037 42111037 single base substitution C T upstream_gene_variant COCA-CN 15 42111745 42111745 single base substitution C G downstream_gene_variant COCA-CN 15 42111745 42111745 single base substitution C G exon_variant COCA-CN 15 42111745 42111745 single base substitution C G intron_variant COCA-CN 15 42111745 42111745 single base substitution C G upstream_gene_variant COCA-CN 15 42111746 42111746 single base substitution G A downstream_gene_variant COCA-CN 15 42111746 42111746 single base substitution G A exon_variant COCA-CN 15 42111746 42111746 single base substitution G A intron_variant COCA-CN 15 42111746 42111746 single base substitution G A upstream_gene_variant COCA-CN 15 42111753 42111753 single base substitution G A downstream_gene_variant COCA-CN 15 42111753 42111753 single base substitution G A exon_variant COCA-CN 15 42111753 42111753 single base substitution G A intron_variant COCA-CN 15 42111753 42111753 single base substitution G A upstream_gene_variant COCA-CN 15 42114586 42114586 single base substitution G T 3_prime_UTR_variant COCA-CN 15 42114586 42114586 single base substitution G T downstream_gene_variant COCA-CN 15 42114586 42114586 single base substitution G T exon_variant COCA-CN 15 42114586 42114586 single base substitution G T missense_variant Q1065H 3195G>T COCA-CN 15 42114586 42114586 single base substitution G T missense_variant Q1071H 3213G>T COCA-CN 15 42114586 42114586 single base substitution G T missense_variant Q904H 2712G>T COCA-CN 15 42114586 42114586 single base substitution G T missense_variant Q948H 2844G>T COCA-CN 15 42114586 42114586 single base substitution G T upstream_gene_variant COCA-CN 15 42115150 42115150 single base substitution T C 3_prime_UTR_variant COCA-CN 15 42115150 42115150 single base substitution T C downstream_gene_variant COCA-CN 15 42115150 42115150 single base substitution T C exon_variant COCA-CN 15 42115150 42115150 single base substitution T C missense_variant S1110P 3328T>C COCA-CN 15 42115150 42115150 single base substitution T C missense_variant S1116P 3346T>C COCA-CN 15 42115150 42115150 single base substitution T C missense_variant S949P 2845T>C COCA-CN 15 42115150 42115150 single base substitution T C missense_variant S993P 2977T>C COCA-CN 15 42116788 42116788 single base substitution G A downstream_gene_variant COCA-CN 15 42116788 42116788 single base substitution G A intron_variant COCA-CN 15 42120437 42120437 single base substitution C G downstream_gene_variant ESAD-UK 15 42063572 42063572 single base substitution G A upstream_gene_variant ESAD-UK 15 42063676 42063676 single base substitution G A upstream_gene_variant ESAD-UK 15 42064695 42064695 single base substitution C T upstream_gene_variant ESAD-UK 15 42065834 42065834 single base substitution C T upstream_gene_variant ESAD-UK 15 42066185 42066185 single base substitution C T upstream_gene_variant ESAD-UK 15 42076165 42076165 single base substitution C A intron_variant ESAD-UK 15 42077651 42077651 single base substitution G C intron_variant ESAD-UK 15 42081015 42081015 single base substitution A G intron_variant ESAD-UK 15 42085654 42085654 single base substitution C G intron_variant ESAD-UK 15 42085665 42085665 single base substitution C T intron_variant ESAD-UK 15 42085779 42085779 single base substitution T C intron_variant ESAD-UK 15 42086582 42086582 single base substitution C T intron_variant ESAD-UK 15 42086911 42086911 single base substitution A G intron_variant ESAD-UK 15 42088049 42088049 single base substitution C T intron_variant ESAD-UK 15 42089531 42089531 single base substitution A G intron_variant ESAD-UK 15 42091883 42091883 single base substitution G A intron_variant ESAD-UK 15 42093821 42093821 single base substitution G A intron_variant ESAD-UK 15 42095656 42095656 single base substitution G A intron_variant ESAD-UK 15 42097963 42097963 single base substitution A G intron_variant ESAD-UK 15 42097963 42097963 single base substitution A G upstream_gene_variant ESAD-UK 15 42098064 42098064 single base substitution G C intron_variant ESAD-UK 15 42098064 42098064 single base substitution G C upstream_gene_variant ESAD-UK 15 42098071 42098071 single base substitution C A intron_variant ESAD-UK 15 42098071 42098071 single base substitution C A upstream_gene_variant ESAD-UK 15 42099419 42099419 insertion of <=200bp - AC intron_variant ESAD-UK 15 42099419 42099419 insertion of <=200bp - AC upstream_gene_variant ESAD-UK 15 42100160 42100160 single base substitution G A intron_variant ESAD-UK 15 42100160 42100160 single base substitution G A upstream_gene_variant ESAD-UK 15 42100817 42100817 single base substitution G A intron_variant ESAD-UK 15 42100817 42100817 single base substitution G A upstream_gene_variant ESAD-UK 15 42103783 42103783 single base substitution G C downstream_gene_variant ESAD-UK 15 42103783 42103783 single base substitution G C exon_variant ESAD-UK 15 42103783 42103783 single base substitution G C intron_variant ESAD-UK 15 42103783 42103783 single base substitution G C upstream_gene_variant ESAD-UK 15 42104098 42104098 single base substitution G A downstream_gene_variant ESAD-UK 15 42104098 42104098 single base substitution G A intron_variant ESAD-UK 15 42104098 42104098 single base substitution G A upstream_gene_variant ESAD-UK 15 42105885 42105885 single base substitution G A 3_prime_UTR_variant ESAD-UK 15 42105885 42105885 single base substitution G A downstream_gene_variant ESAD-UK 15 42105885 42105885 single base substitution G A exon_variant ESAD-UK 15 42105885 42105885 single base substitution G A intron_variant ESAD-UK 15 42105885 42105885 single base substitution G A missense_variant V184M 550G>A ESAD-UK 15 42105885 42105885 single base substitution G A missense_variant V296M 886G>A ESAD-UK 15 42105885 42105885 single base substitution G A missense_variant V302M 904G>A ESAD-UK 15 42105885 42105885 single base substitution G A upstream_gene_variant ESAD-UK 15 42105918 42105918 single base substitution C G 3_prime_UTR_variant ESAD-UK 15 42105918 42105918 single base substitution C G downstream_gene_variant ESAD-UK 15 42105918 42105918 single base substitution C G exon_variant ESAD-UK 15 42105918 42105918 single base substitution C G intron_variant ESAD-UK 15 42105918 42105918 single base substitution C G missense_variant L195V 583C>G ESAD-UK 15 42105918 42105918 single base substitution C G missense_variant L307V 919C>G ESAD-UK 15 42105918 42105918 single base substitution C G missense_variant L313V 937C>G ESAD-UK 15 42105918 42105918 single base substitution C G upstream_gene_variant ESAD-UK 15 42106288 42106288 single base substitution G A downstream_gene_variant ESAD-UK 15 42106288 42106288 single base substitution G A intron_variant ESAD-UK 15 42106288 42106288 single base substitution G A upstream_gene_variant ESAD-UK 15 42107922 42107922 single base substitution G A 3_prime_UTR_variant ESAD-UK 15 42107922 42107922 single base substitution G A downstream_gene_variant ESAD-UK 15 42107922 42107922 single base substitution G A exon_variant ESAD-UK 15 42107922 42107922 single base substitution G A missense_variant R312H 935G>A ESAD-UK 15 42107922 42107922 single base substitution G A missense_variant R356H 1067G>A ESAD-UK 15 42107922 42107922 single base substitution G A missense_variant R473H 1418G>A ESAD-UK 15 42107922 42107922 single base substitution G A missense_variant R479H 1436G>A ESAD-UK 15 42107922 42107922 single base substitution G A upstream_gene_variant ESAD-UK 15 42109193 42109193 single base substitution G T 3_prime_UTR_variant ESAD-UK 15 42109193 42109193 single base substitution G T downstream_gene_variant ESAD-UK 15 42109193 42109193 single base substitution G T exon_variant ESAD-UK 15 42109193 42109193 single base substitution G T synonymous_variant L396L 1188G>T ESAD-UK 15 42109193 42109193 single base substitution G T synonymous_variant L440L 1320G>T ESAD-UK 15 42109193 42109193 single base substitution G T synonymous_variant L557L 1671G>T ESAD-UK 15 42109193 42109193 single base substitution G T synonymous_variant L563L 1689G>T ESAD-UK 15 42109193 42109193 single base substitution G T upstream_gene_variant ESAD-UK 15 42111194 42111194 single base substitution A G downstream_gene_variant ESAD-UK 15 42111194 42111194 single base substitution A G intron_variant ESAD-UK 15 42111194 42111194 single base substitution A G upstream_gene_variant ESAD-UK 15 42115464 42115464 single base substitution G T downstream_gene_variant ESAD-UK 15 42115464 42115464 single base substitution G T intron_variant ESAD-UK 15 42115869 42115869 single base substitution C T 3_prime_UTR_variant ESAD-UK 15 42115869 42115869 single base substitution C T downstream_gene_variant ESAD-UK 15 42115869 42115869 single base substitution C T exon_variant ESAD-UK 15 42115869 42115869 single base substitution C T intron_variant ESAD-UK 15 42115869 42115869 single base substitution C T stop_gained R1114* 3340C>T ESAD-UK 15 42115869 42115869 single base substitution C T stop_gained R1158* 3472C>T ESAD-UK 15 42115869 42115869 single base substitution C T stop_gained R1275* 3823C>T ESAD-UK 15 42115869 42115869 single base substitution C T stop_gained R1281* 3841C>T ESAD-UK 15 42116730 42116730 single base substitution G A 3_prime_UTR_variant ESAD-UK 15 42116730 42116730 single base substitution G A downstream_gene_variant ESAD-UK 15 42116730 42116730 single base substitution G A exon_variant ESAD-UK 15 42116730 42116730 single base substitution G A missense_variant R1144H 3431G>A ESAD-UK 15 42116730 42116730 single base substitution G A missense_variant R1260H 3779G>A ESAD-UK 15 42116730 42116730 single base substitution G A missense_variant R1304H 3911G>A ESAD-UK 15 42116730 42116730 single base substitution G A missense_variant R1421H 4262G>A ESAD-UK 15 42116730 42116730 single base substitution G A missense_variant R1427H 4280G>A ESAD-UK 15 42119038 42119038 single base substitution G A 3_prime_UTR_variant ESAD-UK 15 42119038 42119038 single base substitution G A downstream_gene_variant ESAD-UK 15 42119963 42119963 single base substitution C T 3_prime_UTR_variant ESAD-UK 15 42119963 42119963 single base substitution C T downstream_gene_variant ESAD-UK 15 42120502 42120502 single base substitution G C downstream_gene_variant ESCA-CN 15 42110437 42110437 single base substitution G A 3_prime_UTR_variant ESCA-CN 15 42110437 42110437 single base substitution G A downstream_gene_variant ESCA-CN 15 42110437 42110437 single base substitution G A exon_variant ESCA-CN 15 42110437 42110437 single base substitution G A missense_variant D515N 1543G>A ESCA-CN 15 42110437 42110437 single base substitution G A missense_variant D559N 1675G>A ESCA-CN 15 42110437 42110437 single base substitution G A missense_variant D676N 2026G>A ESCA-CN 15 42110437 42110437 single base substitution G A missense_variant D682N 2044G>A ESCA-CN 15 42110437 42110437 single base substitution G A upstream_gene_variant ESCA-CN 15 42118123 42118123 single base substitution G C 3_prime_UTR_variant ESCA-CN 15 42118123 42118123 single base substitution G C downstream_gene_variant ESCA-CN 15 42118123 42118123 single base substitution G C exon_variant ESCA-CN 15 42120449 42120449 single base substitution T C downstream_gene_variant GBM-US 15 42067489 42067489 single base substitution T G 5_prime_UTR_variant GBM-US 15 42067489 42067489 single base substitution T G exon_variant GBM-US 15 42067489 42067489 single base substitution T G missense_variant S6A 16T>G GBM-US 15 42067489 42067489 single base substitution T G upstream_gene_variant GBM-US 15 42106769 42106769 single base substitution G A 3_prime_UTR_variant GBM-US 15 42106769 42106769 single base substitution G A downstream_gene_variant GBM-US 15 42106769 42106769 single base substitution G A exon_variant GBM-US 15 42106769 42106769 single base substitution G A intron_variant GBM-US 15 42106769 42106769 single base substitution G A synonymous_variant A222A 666G>A GBM-US 15 42106769 42106769 single base substitution G A synonymous_variant A334A 1002G>A GBM-US 15 42106769 42106769 single base substitution G A synonymous_variant A340A 1020G>A GBM-US 15 42106769 42106769 single base substitution G A upstream_gene_variant GBM-US 15 42107465 42107465 single base substitution C T downstream_gene_variant GBM-US 15 42107465 42107465 single base substitution C T exon_variant GBM-US 15 42107465 42107465 single base substitution C T intron_variant GBM-US 15 42107465 42107465 single base substitution C T synonymous_variant P276P 828C>T GBM-US 15 42107465 42107465 single base substitution C T synonymous_variant P393P 1179C>T GBM-US 15 42107465 42107465 single base substitution C T synonymous_variant P399P 1197C>T GBM-US 15 42107465 42107465 single base substitution C T upstream_gene_variant GBM-US 15 42109162 42109162 single base substitution C T 3_prime_UTR_variant GBM-US 15 42109162 42109162 single base substitution C T downstream_gene_variant GBM-US 15 42109162 42109162 single base substitution C T exon_variant GBM-US 15 42109162 42109162 single base substitution C T missense_variant A386V 1157C>T GBM-US 15 42109162 42109162 single base substitution C T missense_variant A430V 1289C>T GBM-US 15 42109162 42109162 single base substitution C T missense_variant A547V 1640C>T GBM-US 15 42109162 42109162 single base substitution C T missense_variant A553V 1658C>T GBM-US 15 42109162 42109162 single base substitution C T upstream_gene_variant GBM-US 15 42111074 42111074 single base substitution G A 3_prime_UTR_variant GBM-US 15 42111074 42111074 single base substitution G A downstream_gene_variant GBM-US 15 42111074 42111074 single base substitution G A exon_variant GBM-US 15 42111074 42111074 single base substitution G A missense_variant R576H 1727G>A GBM-US 15 42111074 42111074 single base substitution G A missense_variant R620H 1859G>A GBM-US 15 42111074 42111074 single base substitution G A missense_variant R737H 2210G>A GBM-US 15 42111074 42111074 single base substitution G A missense_variant R743H 2228G>A GBM-US 15 42111074 42111074 single base substitution G A upstream_gene_variant GBM-US 15 42111153 42111153 single base substitution C T downstream_gene_variant GBM-US 15 42111153 42111153 single base substitution C T splice_region_variant GBM-US 15 42111153 42111153 single base substitution C T upstream_gene_variant KIRC-US 15 42107967 42107967 single base substitution T A 3_prime_UTR_variant KIRC-US 15 42107967 42107967 single base substitution T A downstream_gene_variant KIRC-US 15 42107967 42107967 single base substitution T A exon_variant KIRC-US 15 42107967 42107967 single base substitution T A missense_variant L327Q 980T>A KIRC-US 15 42107967 42107967 single base substitution T A missense_variant L371Q 1112T>A KIRC-US 15 42107967 42107967 single base substitution T A missense_variant L488Q 1463T>A KIRC-US 15 42107967 42107967 single base substitution T A missense_variant L494Q 1481T>A KIRC-US 15 42107967 42107967 single base substitution T A upstream_gene_variant KIRC-US 15 42108803 42108803 single base substitution C A 3_prime_UTR_variant KIRC-US 15 42108803 42108803 single base substitution C A downstream_gene_variant KIRC-US 15 42108803 42108803 single base substitution C A exon_variant KIRC-US 15 42108803 42108803 single base substitution C A missense_variant H353N 1057C>A KIRC-US 15 42108803 42108803 single base substitution C A missense_variant H397N 1189C>A KIRC-US 15 42108803 42108803 single base substitution C A missense_variant H514N 1540C>A KIRC-US 15 42108803 42108803 single base substitution C A missense_variant H520N 1558C>A KIRC-US 15 42108803 42108803 single base substitution C A upstream_gene_variant KIRP-US 15 42105966 42105966 single base substitution G A 3_prime_UTR_variant KIRP-US 15 42105966 42105966 single base substitution G A downstream_gene_variant KIRP-US 15 42105966 42105966 single base substitution G A exon_variant KIRP-US 15 42105966 42105966 single base substitution G A intron_variant KIRP-US 15 42105966 42105966 single base substitution G A missense_variant V211I 631G>A KIRP-US 15 42105966 42105966 single base substitution G A missense_variant V323I 967G>A KIRP-US 15 42105966 42105966 single base substitution G A missense_variant V329I 985G>A KIRP-US 15 42105966 42105966 single base substitution G A upstream_gene_variant LAML-KR 15 42095632 42095632 single base substitution A G intron_variant LAML-KR 15 42103210 42103210 single base substitution G C intron_variant LICA-CN 15 42106817 42106817 single base substitution T G 3_prime_UTR_variant LICA-CN 15 42106817 42106817 single base substitution T G downstream_gene_variant LICA-CN 15 42106817 42106817 single base substitution T G exon_variant LICA-CN 15 42106817 42106817 single base substitution T G intron_variant LICA-CN 15 42106817 42106817 single base substitution T G missense_variant N238K 714T>G LICA-CN 15 42106817 42106817 single base substitution T G missense_variant N350K 1050T>G LICA-CN 15 42106817 42106817 single base substitution T G missense_variant N356K 1068T>G LICA-CN 15 42106817 42106817 single base substitution T G upstream_gene_variant LICA-CN 15 42116745 42116745 single base substitution A T 3_prime_UTR_variant LICA-CN 15 42116745 42116745 single base substitution A T downstream_gene_variant LICA-CN 15 42116745 42116745 single base substitution A T exon_variant LICA-CN 15 42116745 42116745 single base substitution A T missense_variant Q1149L 3446A>T LICA-CN 15 42116745 42116745 single base substitution A T missense_variant Q1265L 3794A>T LICA-CN 15 42116745 42116745 single base substitution A T missense_variant Q1309L 3926A>T LICA-CN 15 42116745 42116745 single base substitution A T missense_variant Q1426L 4277A>T LICA-CN 15 42116745 42116745 single base substitution A T missense_variant Q1432L 4295A>T LICA-FR 15 42066755 42066755 single base substitution G A 5_prime_UTR_variant LICA-FR 15 42066755 42066755 single base substitution G A exon_variant LICA-FR 15 42066755 42066755 single base substitution G A upstream_gene_variant LICA-FR 15 42096718 42096718 single base substitution A G intron_variant LICA-FR 15 42106767 42106767 single base substitution G A 3_prime_UTR_variant LICA-FR 15 42106767 42106767 single base substitution G A downstream_gene_variant LICA-FR 15 42106767 42106767 single base substitution G A exon_variant LICA-FR 15 42106767 42106767 single base substitution G A intron_variant LICA-FR 15 42106767 42106767 single base substitution G A missense_variant A222T 664G>A LICA-FR 15 42106767 42106767 single base substitution G A missense_variant A334T 1000G>A LICA-FR 15 42106767 42106767 single base substitution G A missense_variant A340T 1018G>A LICA-FR 15 42106767 42106767 single base substitution G A upstream_gene_variant LICA-FR 15 42109850 42109850 single base substitution G A 3_prime_UTR_variant LICA-FR 15 42109850 42109850 single base substitution G A downstream_gene_variant LICA-FR 15 42109850 42109850 single base substitution G A exon_variant LICA-FR 15 42109850 42109850 single base substitution G A synonymous_variant V446V 1338G>A LICA-FR 15 42109850 42109850 single base substitution G A synonymous_variant V490V 1470G>A LICA-FR 15 42109850 42109850 single base substitution G A synonymous_variant V607V 1821G>A LICA-FR 15 42109850 42109850 single base substitution G A synonymous_variant V613V 1839G>A LICA-FR 15 42109850 42109850 single base substitution G A upstream_gene_variant LIHC-US 15 42104835 42104835 single base substitution A G 3_prime_UTR_variant LIHC-US 15 42104835 42104835 single base substitution A G downstream_gene_variant LIHC-US 15 42104835 42104835 single base substitution A G exon_variant LIHC-US 15 42104835 42104835 single base substitution A G missense_variant D207G 620A>G LIHC-US 15 42104835 42104835 single base substitution A G missense_variant D95G 284A>G LIHC-US 15 42104835 42104835 single base substitution A G upstream_gene_variant LIHC-US 15 42110257 42110257 deletion of <=200bp A - 3_prime_UTR_variant LIHC-US 15 42110257 42110257 deletion of <=200bp A - downstream_gene_variant LIHC-US 15 42110257 42110257 deletion of <=200bp A - exon_variant LIHC-US 15 42110257 42110257 deletion of <=200bp A - frameshift_variant Q491 LIHC-US 15 42110257 42110257 deletion of <=200bp A - frameshift_variant Q535 LIHC-US 15 42110257 42110257 deletion of <=200bp A - frameshift_variant Q652 LIHC-US 15 42110257 42110257 deletion of <=200bp A - frameshift_variant Q658 LIHC-US 15 42110257 42110257 deletion of <=200bp A - upstream_gene_variant LIHC-US 15 42115228 42115228 single base substitution G A 3_prime_UTR_variant LIHC-US 15 42115228 42115228 single base substitution G A downstream_gene_variant LIHC-US 15 42115228 42115228 single base substitution G A exon_variant LIHC-US 15 42115228 42115228 single base substitution G A intron_variant LIHC-US 15 42115228 42115228 single base substitution G A missense_variant A1019T 3055G>A LIHC-US 15 42115228 42115228 single base substitution G A missense_variant A1136T 3406G>A LIHC-US 15 42115228 42115228 single base substitution G A missense_variant A1142T 3424G>A LIHC-US 15 42115228 42115228 single base substitution G A missense_variant A975T 2923G>A LINC-JP 15 42104884 42104884 single base substitution G A downstream_gene_variant LINC-JP 15 42104884 42104884 single base substitution G A exon_variant LINC-JP 15 42104884 42104884 single base substitution G A intron_variant LINC-JP 15 42104884 42104884 single base substitution G A upstream_gene_variant LINC-JP 15 42109073 42109073 single base substitution G A downstream_gene_variant LINC-JP 15 42109073 42109073 single base substitution G A intron_variant LINC-JP 15 42109073 42109073 single base substitution G A upstream_gene_variant LINC-JP 15 42109647 42109647 single base substitution T A 3_prime_UTR_variant LINC-JP 15 42109647 42109647 single base substitution T A downstream_gene_variant LINC-JP 15 42109647 42109647 single base substitution T A exon_variant LINC-JP 15 42109647 42109647 single base substitution T A synonymous_variant T430T 1290T>A LINC-JP 15 42109647 42109647 single base substitution T A synonymous_variant T474T 1422T>A LINC-JP 15 42109647 42109647 single base substitution T A synonymous_variant T591T 1773T>A LINC-JP 15 42109647 42109647 single base substitution T A synonymous_variant T597T 1791T>A LINC-JP 15 42109647 42109647 single base substitution T A upstream_gene_variant LINC-JP 15 42112474 42112474 single base substitution A G downstream_gene_variant LINC-JP 15 42112474 42112474 single base substitution A G intron_variant LINC-JP 15 42112474 42112474 single base substitution A G upstream_gene_variant LINC-JP 15 42113273 42113273 single base substitution C G downstream_gene_variant LINC-JP 15 42113273 42113273 single base substitution C G splice_region_variant LINC-JP 15 42113273 42113273 single base substitution C G upstream_gene_variant LINC-JP 15 42113984 42113984 single base substitution G A downstream_gene_variant LINC-JP 15 42113984 42113984 single base substitution G A intron_variant LINC-JP 15 42113984 42113984 single base substitution G A upstream_gene_variant LINC-JP 15 42114621 42114621 single base substitution G C downstream_gene_variant LINC-JP 15 42114621 42114621 single base substitution G C exon_variant LINC-JP 15 42114621 42114621 single base substitution G C splice_donor_variant LINC-JP 15 42114621 42114621 single base substitution G C upstream_gene_variant LINC-JP 15 42115899 42115899 single base substitution C G 3_prime_UTR_variant LINC-JP 15 42115899 42115899 single base substitution C G downstream_gene_variant LINC-JP 15 42115899 42115899 single base substitution C G exon_variant LINC-JP 15 42115899 42115899 single base substitution C G intron_variant LINC-JP 15 42115899 42115899 single base substitution C G missense_variant P1124A 3370C>G LINC-JP 15 42115899 42115899 single base substitution C G missense_variant P1168A 3502C>G LINC-JP 15 42115899 42115899 single base substitution C G missense_variant P1285A 3853C>G LINC-JP 15 42115899 42115899 single base substitution C G missense_variant P1291A 3871C>G LINC-JP 15 42117529 42117529 single base substitution C A 3_prime_UTR_variant LINC-JP 15 42117529 42117529 single base substitution C A downstream_gene_variant LINC-JP 15 42117529 42117529 single base substitution C A exon_variant LINC-JP 15 42117529 42117529 single base substitution C A synonymous_variant G1197G 3591C>A LINC-JP 15 42117529 42117529 single base substitution C A synonymous_variant G1313G 3939C>A LINC-JP 15 42117529 42117529 single base substitution C A synonymous_variant G1357G 4071C>A LINC-JP 15 42117529 42117529 single base substitution C A synonymous_variant G1474G 4422C>A LINC-JP 15 42117529 42117529 single base substitution C A synonymous_variant G1480G 4440C>A LINC-JP 15 42117633 42117633 single base substitution G A 3_prime_UTR_variant LINC-JP 15 42117633 42117633 single base substitution G A downstream_gene_variant LINC-JP 15 42117633 42117633 single base substitution G A exon_variant LINC-JP 15 42117633 42117633 single base substitution G A stop_retained_variant *1232* 3695G>A LINC-JP 15 42117633 42117633 single base substitution G A stop_retained_variant *1348* 4043G>A LINC-JP 15 42117633 42117633 single base substitution G A stop_retained_variant *1392* 4175G>A LINC-JP 15 42117633 42117633 single base substitution G A stop_retained_variant *1509* 4526G>A LINC-JP 15 42117633 42117633 single base substitution G A stop_retained_variant *1515* 4544G>A LINC-JP 15 42121375 42121375 single base substitution G C downstream_gene_variant LIRI-JP 15 42062073 42062073 single base substitution A T upstream_gene_variant LIRI-JP 15 42062142 42062142 single base substitution C G upstream_gene_variant LIRI-JP 15 42062262 42062262 single base substitution C T upstream_gene_variant LIRI-JP 15 42064294 42064294 single base substitution G A upstream_gene_variant LIRI-JP 15 42066508 42066508 single base substitution G A upstream_gene_variant LIRI-JP 15 42066508 42066508 single base substitution G C upstream_gene_variant LIRI-JP 15 42072942 42072942 single base substitution T A intron_variant LIRI-JP 15 42073099 42073099 single base substitution T C intron_variant LIRI-JP 15 42077442 42077442 single base substitution A G intron_variant LIRI-JP 15 42078290 42078290 single base substitution A G intron_variant LIRI-JP 15 42079458 42079458 single base substitution A T intron_variant LIRI-JP 15 42079684 42079684 single base substitution G T intron_variant LIRI-JP 15 42080407 42080407 single base substitution G C intron_variant LIRI-JP 15 42081183 42081183 single base substitution A G intron_variant LIRI-JP 15 42081357 42081357 single base substitution A G intron_variant LIRI-JP 15 42084646 42084646 single base substitution A T intron_variant LIRI-JP 15 42085221 42085221 single base substitution C T intron_variant LIRI-JP 15 42085559 42085559 single base substitution C T intron_variant LIRI-JP 15 42085560 42085560 single base substitution C A intron_variant LIRI-JP 15 42086813 42086813 single base substitution A G intron_variant LIRI-JP 15 42090952 42090952 single base substitution T G intron_variant LIRI-JP 15 42091227 42091227 single base substitution C G intron_variant LIRI-JP 15 42093584 42093584 single base substitution T C intron_variant LIRI-JP 15 42095413 42095413 single base substitution G C intron_variant LIRI-JP 15 42096956 42096956 single base substitution C T intron_variant LIRI-JP 15 42099412 42099412 single base substitution T G intron_variant LIRI-JP 15 42099412 42099412 single base substitution T G upstream_gene_variant LIRI-JP 15 42100220 42100220 single base substitution G T intron_variant LIRI-JP 15 42100220 42100220 single base substitution G T upstream_gene_variant LIRI-JP 15 42105008 42105008 single base substitution C T downstream_gene_variant LIRI-JP 15 42105008 42105008 single base substitution C T exon_variant LIRI-JP 15 42105008 42105008 single base substitution C T intron_variant LIRI-JP 15 42105008 42105008 single base substitution C T upstream_gene_variant LIRI-JP 15 42105034 42105034 single base substitution C T downstream_gene_variant LIRI-JP 15 42105034 42105034 single base substitution C T exon_variant LIRI-JP 15 42105034 42105034 single base substitution C T intron_variant LIRI-JP 15 42105034 42105034 single base substitution C T upstream_gene_variant LIRI-JP 15 42105080 42105080 single base substitution G A downstream_gene_variant LIRI-JP 15 42105080 42105080 single base substitution G A exon_variant LIRI-JP 15 42105080 42105080 single base substitution G A intron_variant LIRI-JP 15 42105080 42105080 single base substitution G A upstream_gene_variant LIRI-JP 15 42105506 42105506 single base substitution C A downstream_gene_variant LIRI-JP 15 42105506 42105506 single base substitution C A exon_variant LIRI-JP 15 42105506 42105506 single base substitution C A intron_variant LIRI-JP 15 42105506 42105506 single base substitution C A upstream_gene_variant LIRI-JP 15 42106658 42106658 single base substitution G A downstream_gene_variant LIRI-JP 15 42106658 42106658 single base substitution G A intron_variant LIRI-JP 15 42106658 42106658 single base substitution G A upstream_gene_variant LIRI-JP 15 42107247 42107247 single base substitution G T downstream_gene_variant LIRI-JP 15 42107247 42107247 single base substitution G T intron_variant LIRI-JP 15 42107247 42107247 single base substitution G T upstream_gene_variant LIRI-JP 15 42107870 42107870 single base substitution G T 3_prime_UTR_variant LIRI-JP 15 42107870 42107870 single base substitution G T downstream_gene_variant LIRI-JP 15 42107870 42107870 single base substitution G T exon_variant LIRI-JP 15 42107870 42107870 single base substitution G T missense_variant D295Y 883G>T LIRI-JP 15 42107870 42107870 single base substitution G T missense_variant D339Y 1015G>T LIRI-JP 15 42107870 42107870 single base substitution G T missense_variant D456Y 1366G>T LIRI-JP 15 42107870 42107870 single base substitution G T missense_variant D462Y 1384G>T LIRI-JP 15 42107870 42107870 single base substitution G T upstream_gene_variant LIRI-JP 15 42108252 42108252 single base substitution T G downstream_gene_variant LIRI-JP 15 42108252 42108252 single base substitution T G intron_variant LIRI-JP 15 42108252 42108252 single base substitution T G upstream_gene_variant LIRI-JP 15 42110240 42110240 single base substitution G A 3_prime_UTR_variant LIRI-JP 15 42110240 42110240 single base substitution G A downstream_gene_variant LIRI-JP 15 42110240 42110240 single base substitution G A exon_variant LIRI-JP 15 42110240 42110240 single base substitution G A synonymous_variant K485K 1455G>A LIRI-JP 15 42110240 42110240 single base substitution G A synonymous_variant K529K 1587G>A LIRI-JP 15 42110240 42110240 single base substitution G A synonymous_variant K646K 1938G>A LIRI-JP 15 42110240 42110240 single base substitution G A synonymous_variant K652K 1956G>A LIRI-JP 15 42110240 42110240 single base substitution G A upstream_gene_variant LIRI-JP 15 42111791 42111791 single base substitution A G downstream_gene_variant LIRI-JP 15 42111791 42111791 single base substitution A G exon_variant LIRI-JP 15 42111791 42111791 single base substitution A G splice_acceptor_variant LIRI-JP 15 42111791 42111791 single base substitution A G upstream_gene_variant LIRI-JP 15 42115472 42115472 single base substitution G A downstream_gene_variant LIRI-JP 15 42115472 42115472 single base substitution G A intron_variant LIRI-JP 15 42116135 42116135 single base substitution T C 3_prime_UTR_variant LIRI-JP 15 42116135 42116135 single base substitution T C downstream_gene_variant LIRI-JP 15 42116135 42116135 single base substitution T C exon_variant LIRI-JP 15 42116135 42116135 single base substitution T C intron_variant LIRI-JP 15 42116135 42116135 single base substitution T C synonymous_variant C1202C 3606T>C LIRI-JP 15 42116135 42116135 single base substitution T C synonymous_variant C1246C 3738T>C LIRI-JP 15 42116135 42116135 single base substitution T C synonymous_variant C1363C 4089T>C LIRI-JP 15 42116135 42116135 single base substitution T C synonymous_variant C1369C 4107T>C LIRI-JP 15 42118120 42118120 deletion of <=200bp C - 3_prime_UTR_variant LIRI-JP 15 42118120 42118120 deletion of <=200bp C - downstream_gene_variant LIRI-JP 15 42118120 42118120 deletion of <=200bp C - exon_variant LIRI-JP 15 42118161 42118161 single base substitution A T 3_prime_UTR_variant LIRI-JP 15 42118161 42118161 single base substitution A T downstream_gene_variant LIRI-JP 15 42118161 42118161 single base substitution A T exon_variant LIRI-JP 15 42121885 42121885 single base substitution C T downstream_gene_variant LUSC-KR 15 42066583 42066583 single base substitution C G upstream_gene_variant LUSC-KR 15 42070354 42070354 single base substitution T C intron_variant LUSC-KR 15 42083901 42083901 single base substitution T A intron_variant LUSC-KR 15 42091533 42091533 single base substitution G C intron_variant LUSC-KR 15 42092591 42092591 single base substitution G T intron_variant LUSC-KR 15 42095170 42095170 single base substitution G C intron_variant LUSC-KR 15 42095632 42095632 single base substitution A G intron_variant LUSC-KR 15 42100398 42100398 single base substitution G T intron_variant LUSC-KR 15 42100398 42100398 single base substitution G T upstream_gene_variant LUSC-KR 15 42107463 42107463 single base substitution C T downstream_gene_variant LUSC-KR 15 42107463 42107463 single base substitution C T exon_variant LUSC-KR 15 42107463 42107463 single base substitution C T intron_variant LUSC-KR 15 42107463 42107463 single base substitution C T missense_variant P276S 826C>T LUSC-KR 15 42107463 42107463 single base substitution C T missense_variant P393S 1177C>T LUSC-KR 15 42107463 42107463 single base substitution C T missense_variant P399S 1195C>T LUSC-KR 15 42107463 42107463 single base substitution C T upstream_gene_variant LUSC-KR 15 42109223 42109223 single base substitution T C 3_prime_UTR_variant LUSC-KR 15 42109223 42109223 single base substitution T C downstream_gene_variant LUSC-KR 15 42109223 42109223 single base substitution T C exon_variant LUSC-KR 15 42109223 42109223 single base substitution T C synonymous_variant V406V 1218T>C LUSC-KR 15 42109223 42109223 single base substitution T C synonymous_variant V450V 1350T>C LUSC-KR 15 42109223 42109223 single base substitution T C synonymous_variant V567V 1701T>C LUSC-KR 15 42109223 42109223 single base substitution T C synonymous_variant V573V 1719T>C LUSC-KR 15 42109223 42109223 single base substitution T C upstream_gene_variant LUSC-KR 15 42109975 42109975 single base substitution T G downstream_gene_variant LUSC-KR 15 42109975 42109975 single base substitution T G intron_variant LUSC-KR 15 42109975 42109975 single base substitution T G upstream_gene_variant LUSC-KR 15 42111298 42111298 single base substitution C G downstream_gene_variant LUSC-KR 15 42111298 42111298 single base substitution C G intron_variant LUSC-KR 15 42111298 42111298 single base substitution C G upstream_gene_variant LUSC-KR 15 42112172 42112172 single base substitution G A downstream_gene_variant LUSC-KR 15 42112172 42112172 single base substitution G A intron_variant LUSC-KR 15 42112172 42112172 single base substitution G A upstream_gene_variant LUSC-KR 15 42114414 42114414 single base substitution C T intron_variant LUSC-KR 15 42114414 42114414 single base substitution C T upstream_gene_variant LUSC-KR 15 42115426 42115426 single base substitution A G downstream_gene_variant LUSC-KR 15 42115426 42115426 single base substitution A G intron_variant LUSC-KR 15 42115426 42115426 single base substitution A G splice_region_variant LUSC-KR 15 42115747 42115747 single base substitution G C 3_prime_UTR_variant LUSC-KR 15 42115747 42115747 single base substitution G C downstream_gene_variant LUSC-KR 15 42115747 42115747 single base substitution G C exon_variant LUSC-KR 15 42115747 42115747 single base substitution G C intron_variant LUSC-KR 15 42115747 42115747 single base substitution G C missense_variant R1073P 3218G>C LUSC-KR 15 42115747 42115747 single base substitution G C missense_variant R1117P 3350G>C LUSC-KR 15 42115747 42115747 single base substitution G C missense_variant R1234P 3701G>C LUSC-KR 15 42115747 42115747 single base substitution G C missense_variant R1240P 3719G>C LUSC-KR 15 42117336 42117336 single base substitution A C downstream_gene_variant LUSC-KR 15 42117336 42117336 single base substitution A C intron_variant LUSC-KR 15 42118123 42118123 single base substitution G C 3_prime_UTR_variant LUSC-KR 15 42118123 42118123 single base substitution G C downstream_gene_variant LUSC-KR 15 42118123 42118123 single base substitution G C exon_variant LUSC-KR 15 42118651 42118651 single base substitution T C 3_prime_UTR_variant LUSC-KR 15 42118651 42118651 single base substitution T C downstream_gene_variant LUSC-KR 15 42118971 42118971 single base substitution A G 3_prime_UTR_variant LUSC-KR 15 42118971 42118971 single base substitution A G downstream_gene_variant LUSC-KR 15 42119030 42119030 single base substitution A G 3_prime_UTR_variant LUSC-KR 15 42119030 42119030 single base substitution A G downstream_gene_variant LUSC-KR 15 42119593 42119593 single base substitution C A 3_prime_UTR_variant LUSC-KR 15 42119593 42119593 single base substitution C A downstream_gene_variant LUSC-KR 15 42119603 42119603 single base substitution C T 3_prime_UTR_variant LUSC-KR 15 42119603 42119603 single base substitution C T downstream_gene_variant LUSC-KR 15 42119606 42119606 single base substitution C T 3_prime_UTR_variant LUSC-KR 15 42119606 42119606 single base substitution C T downstream_gene_variant LUSC-KR 15 42119711 42119711 single base substitution G A 3_prime_UTR_variant LUSC-KR 15 42119711 42119711 single base substitution G A downstream_gene_variant LUSC-KR 15 42119900 42119900 single base substitution T C 3_prime_UTR_variant LUSC-KR 15 42119900 42119900 single base substitution T C downstream_gene_variant LUSC-KR 15 42120157 42120157 single base substitution G C downstream_gene_variant LUSC-KR 15 42123421 42123421 single base substitution T C downstream_gene_variant LUSC-US 15 42106796 42106796 single base substitution C T 3_prime_UTR_variant LUSC-US 15 42106796 42106796 single base substitution C T downstream_gene_variant LUSC-US 15 42106796 42106796 single base substitution C T exon_variant LUSC-US 15 42106796 42106796 single base substitution C T intron_variant LUSC-US 15 42106796 42106796 single base substitution C T synonymous_variant A231A 693C>T LUSC-US 15 42106796 42106796 single base substitution C T synonymous_variant A343A 1029C>T LUSC-US 15 42106796 42106796 single base substitution C T synonymous_variant A349A 1047C>T LUSC-US 15 42106796 42106796 single base substitution C T upstream_gene_variant LUSC-US 15 42107463 42107463 single base substitution C T downstream_gene_variant LUSC-US 15 42107463 42107463 single base substitution C T exon_variant LUSC-US 15 42107463 42107463 single base substitution C T intron_variant LUSC-US 15 42107463 42107463 single base substitution C T missense_variant P276S 826C>T LUSC-US 15 42107463 42107463 single base substitution C T missense_variant P393S 1177C>T LUSC-US 15 42107463 42107463 single base substitution C T missense_variant P399S 1195C>T LUSC-US 15 42107463 42107463 single base substitution C T upstream_gene_variant LUSC-US 15 42107464 42107464 single base substitution C T downstream_gene_variant LUSC-US 15 42107464 42107464 single base substitution C T exon_variant LUSC-US 15 42107464 42107464 single base substitution C T intron_variant LUSC-US 15 42107464 42107464 single base substitution C T missense_variant P276L 827C>T LUSC-US 15 42107464 42107464 single base substitution C T missense_variant P393L 1178C>T LUSC-US 15 42107464 42107464 single base substitution C T missense_variant P399L 1196C>T LUSC-US 15 42107464 42107464 single base substitution C T upstream_gene_variant LUSC-US 15 42109934 42109934 single base substitution G T downstream_gene_variant LUSC-US 15 42109934 42109934 single base substitution G T splice_donor_variant LUSC-US 15 42109934 42109934 single base substitution G T upstream_gene_variant MALY-DE 15 42064821 42064829 deletion of <=200bp AAAAAAAAA - upstream_gene_variant MALY-DE 15 42067032 42067032 single base substitution G A 5_prime_UTR_variant MALY-DE 15 42067032 42067032 single base substitution G A intron_variant MALY-DE 15 42067032 42067032 single base substitution G A upstream_gene_variant MALY-DE 15 42072401 42072401 single base substitution T C intron_variant MALY-DE 15 42074313 42074313 single base substitution A T intron_variant MALY-DE 15 42111931 42111931 single base substitution G A downstream_gene_variant MALY-DE 15 42111931 42111931 single base substitution G A intron_variant MALY-DE 15 42111931 42111931 single base substitution G A upstream_gene_variant MELA-AU 15 42062301 42062301 single base substitution C T upstream_gene_variant MELA-AU 15 42063465 42063465 single base substitution G A upstream_gene_variant MELA-AU 15 42063833 42063833 single base substitution G A upstream_gene_variant MELA-AU 15 42064434 42064434 single base substitution A C upstream_gene_variant MELA-AU 15 42064575 42064575 single base substitution C G upstream_gene_variant MELA-AU 15 42064625 42064625 single base substitution A G upstream_gene_variant MELA-AU 15 42064708 42064708 single base substitution C T upstream_gene_variant MELA-AU 15 42065264 42065264 single base substitution C T upstream_gene_variant MELA-AU 15 42066622 42066622 single base substitution C T upstream_gene_variant MELA-AU 15 42067533 42067533 single base substitution C T 5_prime_UTR_variant MELA-AU 15 42067533 42067533 single base substitution C T exon_variant MELA-AU 15 42067533 42067533 single base substitution C T synonymous_variant S20S 60C>T MELA-AU 15 42069493 42069493 single base substitution C T intron_variant MELA-AU 15 42069533 42069533 single base substitution C T intron_variant MELA-AU 15 42070321 42070321 single base substitution C T intron_variant MELA-AU 15 42070964 42070964 single base substitution T G intron_variant MELA-AU 15 42071709 42071709 single base substitution T C intron_variant MELA-AU 15 42071896 42071896 single base substitution A G intron_variant MELA-AU 15 42072122 42072122 single base substitution C T intron_variant MELA-AU 15 42072623 42072623 single base substitution G A intron_variant MELA-AU 15 42072686 42072686 single base substitution C T intron_variant MELA-AU 15 42073604 42073604 single base substitution T G intron_variant MELA-AU 15 42073991 42073991 single base substitution T A intron_variant MELA-AU 15 42074168 42074168 single base substitution C T intron_variant MELA-AU 15 42074646 42074646 single base substitution G A intron_variant MELA-AU 15 42074731 42074732 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 42074802 42074802 single base substitution T G intron_variant MELA-AU 15 42075293 42075293 single base substitution C T intron_variant MELA-AU 15 42075705 42075705 single base substitution C T intron_variant MELA-AU 15 42076067 42076067 single base substitution C G intron_variant MELA-AU 15 42076699 42076699 single base substitution G T intron_variant MELA-AU 15 42076703 42076703 single base substitution C T intron_variant MELA-AU 15 42076862 42076862 single base substitution C T intron_variant MELA-AU 15 42078181 42078181 single base substitution C T intron_variant MELA-AU 15 42078229 42078229 single base substitution C T intron_variant MELA-AU 15 42078674 42078674 single base substitution C T intron_variant MELA-AU 15 42078734 42078735 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42079155 42079156 multiple base substitution (>=2bp and <=200bp) GG AA intron_variant MELA-AU 15 42080980 42080980 single base substitution T G intron_variant MELA-AU 15 42083174 42083174 single base substitution C T intron_variant MELA-AU 15 42083727 42083727 single base substitution C T intron_variant MELA-AU 15 42083788 42083788 single base substitution C T intron_variant MELA-AU 15 42084057 42084057 single base substitution C T intron_variant MELA-AU 15 42084972 42084972 single base substitution C T intron_variant MELA-AU 15 42085170 42085170 single base substitution T C intron_variant MELA-AU 15 42085221 42085221 single base substitution C T intron_variant MELA-AU 15 42085352 42085352 single base substitution T A intron_variant MELA-AU 15 42086315 42086315 single base substitution A G intron_variant MELA-AU 15 42086398 42086399 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 42086742 42086742 single base substitution C T intron_variant MELA-AU 15 42088324 42088324 single base substitution G A intron_variant MELA-AU 15 42089344 42089344 single base substitution G A intron_variant MELA-AU 15 42089484 42089485 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 42090078 42090078 single base substitution T C intron_variant MELA-AU 15 42090169 42090169 single base substitution C T intron_variant MELA-AU 15 42091425 42091425 single base substitution G A intron_variant MELA-AU 15 42091645 42091645 single base substitution C T intron_variant MELA-AU 15 42091972 42091972 single base substitution C T intron_variant MELA-AU 15 42092663 42092663 single base substitution C T intron_variant MELA-AU 15 42093204 42093204 single base substitution A T intron_variant MELA-AU 15 42093848 42093848 single base substitution C T intron_variant MELA-AU 15 42094935 42094935 single base substitution G C intron_variant MELA-AU 15 42094997 42094997 single base substitution A G intron_variant MELA-AU 15 42095867 42095867 single base substitution C T intron_variant MELA-AU 15 42097329 42097329 single base substitution C T intron_variant MELA-AU 15 42097835 42097835 single base substitution C T intron_variant MELA-AU 15 42098169 42098169 single base substitution C T intron_variant MELA-AU 15 42098169 42098169 single base substitution C T upstream_gene_variant MELA-AU 15 42098447 42098447 single base substitution G T intron_variant MELA-AU 15 42098447 42098447 single base substitution G T upstream_gene_variant MELA-AU 15 42098581 42098581 single base substitution C T intron_variant MELA-AU 15 42098581 42098581 single base substitution C T upstream_gene_variant MELA-AU 15 42099306 42099306 single base substitution C T intron_variant MELA-AU 15 42099306 42099306 single base substitution C T upstream_gene_variant MELA-AU 15 42099342 42099342 single base substitution G T intron_variant MELA-AU 15 42099342 42099342 single base substitution G T upstream_gene_variant MELA-AU 15 42100033 42100033 single base substitution T C intron_variant MELA-AU 15 42100033 42100033 single base substitution T C upstream_gene_variant MELA-AU 15 42100424 42100424 single base substitution C T intron_variant MELA-AU 15 42100424 42100424 single base substitution C T upstream_gene_variant MELA-AU 15 42100460 42100460 single base substitution A G intron_variant MELA-AU 15 42100460 42100460 single base substitution A G upstream_gene_variant MELA-AU 15 42101090 42101090 single base substitution C T intron_variant MELA-AU 15 42101090 42101090 single base substitution C T upstream_gene_variant MELA-AU 15 42101721 42101721 single base substitution C T intron_variant MELA-AU 15 42101721 42101721 single base substitution C T upstream_gene_variant MELA-AU 15 42102037 42102037 single base substitution C T intron_variant MELA-AU 15 42102037 42102037 single base substitution C T upstream_gene_variant MELA-AU 15 42102581 42102581 single base substitution C T intron_variant MELA-AU 15 42102581 42102581 single base substitution C T upstream_gene_variant MELA-AU 15 42102987 42102987 single base substitution C T exon_variant MELA-AU 15 42102987 42102987 single base substitution C T intron_variant MELA-AU 15 42103235 42103236 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 42103467 42103467 single base substitution G A exon_variant MELA-AU 15 42103467 42103467 single base substitution G A intron_variant MELA-AU 15 42104255 42104255 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42104255 42104255 single base substitution C T downstream_gene_variant MELA-AU 15 42104255 42104255 single base substitution C T exon_variant MELA-AU 15 42104255 42104255 single base substitution C T missense_variant S143F 428C>T MELA-AU 15 42104255 42104255 single base substitution C T missense_variant S31F 92C>T MELA-AU 15 42104255 42104255 single base substitution C T upstream_gene_variant MELA-AU 15 42104257 42104257 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42104257 42104257 single base substitution C T downstream_gene_variant MELA-AU 15 42104257 42104257 single base substitution C T exon_variant MELA-AU 15 42104257 42104257 single base substitution C T missense_variant P144S 430C>T MELA-AU 15 42104257 42104257 single base substitution C T missense_variant P32S 94C>T MELA-AU 15 42104257 42104257 single base substitution C T upstream_gene_variant MELA-AU 15 42104642 42104642 single base substitution C T downstream_gene_variant MELA-AU 15 42104642 42104642 single base substitution C T intron_variant MELA-AU 15 42104642 42104642 single base substitution C T upstream_gene_variant MELA-AU 15 42104831 42104831 single base substitution G A 3_prime_UTR_variant MELA-AU 15 42104831 42104831 single base substitution G A downstream_gene_variant MELA-AU 15 42104831 42104831 single base substitution G A exon_variant MELA-AU 15 42104831 42104831 single base substitution G A missense_variant D206N 616G>A MELA-AU 15 42104831 42104831 single base substitution G A missense_variant D94N 280G>A MELA-AU 15 42104831 42104831 single base substitution G A upstream_gene_variant MELA-AU 15 42104886 42104886 single base substitution C T downstream_gene_variant MELA-AU 15 42104886 42104886 single base substitution C T exon_variant MELA-AU 15 42104886 42104886 single base substitution C T intron_variant MELA-AU 15 42104886 42104886 single base substitution C T upstream_gene_variant MELA-AU 15 42105009 42105009 single base substitution C T downstream_gene_variant MELA-AU 15 42105009 42105009 single base substitution C T exon_variant MELA-AU 15 42105009 42105009 single base substitution C T intron_variant MELA-AU 15 42105009 42105009 single base substitution C T upstream_gene_variant MELA-AU 15 42105064 42105064 single base substitution C T downstream_gene_variant MELA-AU 15 42105064 42105064 single base substitution C T exon_variant MELA-AU 15 42105064 42105064 single base substitution C T intron_variant MELA-AU 15 42105064 42105064 single base substitution C T upstream_gene_variant MELA-AU 15 42105401 42105401 single base substitution G A downstream_gene_variant MELA-AU 15 42105401 42105401 single base substitution G A exon_variant MELA-AU 15 42105401 42105401 single base substitution G A intron_variant MELA-AU 15 42105401 42105401 single base substitution G A upstream_gene_variant MELA-AU 15 42105506 42105506 single base substitution C T downstream_gene_variant MELA-AU 15 42105506 42105506 single base substitution C T exon_variant MELA-AU 15 42105506 42105506 single base substitution C T intron_variant MELA-AU 15 42105506 42105506 single base substitution C T upstream_gene_variant MELA-AU 15 42105705 42105705 single base substitution C T downstream_gene_variant MELA-AU 15 42105705 42105705 single base substitution C T exon_variant MELA-AU 15 42105705 42105705 single base substitution C T intron_variant MELA-AU 15 42105705 42105705 single base substitution C T upstream_gene_variant MELA-AU 15 42105727 42105727 single base substitution C T downstream_gene_variant MELA-AU 15 42105727 42105727 single base substitution C T exon_variant MELA-AU 15 42105727 42105727 single base substitution C T intron_variant MELA-AU 15 42105727 42105727 single base substitution C T upstream_gene_variant MELA-AU 15 42106158 42106158 single base substitution C T downstream_gene_variant MELA-AU 15 42106158 42106158 single base substitution C T intron_variant MELA-AU 15 42106158 42106158 single base substitution C T upstream_gene_variant MELA-AU 15 42106300 42106300 single base substitution C T downstream_gene_variant MELA-AU 15 42106300 42106300 single base substitution C T intron_variant MELA-AU 15 42106300 42106300 single base substitution C T upstream_gene_variant MELA-AU 15 42106918 42106918 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42106918 42106918 single base substitution C T downstream_gene_variant MELA-AU 15 42106918 42106918 single base substitution C T exon_variant MELA-AU 15 42106918 42106918 single base substitution C T intron_variant MELA-AU 15 42106918 42106918 single base substitution C T missense_variant S272F 815C>T MELA-AU 15 42106918 42106918 single base substitution C T missense_variant S384F 1151C>T MELA-AU 15 42106918 42106918 single base substitution C T missense_variant S390F 1169C>T MELA-AU 15 42106918 42106918 single base substitution C T upstream_gene_variant MELA-AU 15 42107015 42107015 single base substitution C T downstream_gene_variant MELA-AU 15 42107015 42107015 single base substitution C T intron_variant MELA-AU 15 42107015 42107015 single base substitution C T upstream_gene_variant MELA-AU 15 42107182 42107182 single base substitution C T downstream_gene_variant MELA-AU 15 42107182 42107182 single base substitution C T intron_variant MELA-AU 15 42107182 42107182 single base substitution C T upstream_gene_variant MELA-AU 15 42107449 42107449 single base substitution C T downstream_gene_variant MELA-AU 15 42107449 42107449 single base substitution C T intron_variant MELA-AU 15 42107449 42107449 single base substitution C T splice_region_variant MELA-AU 15 42107449 42107449 single base substitution C T upstream_gene_variant MELA-AU 15 42107648 42107648 single base substitution C T downstream_gene_variant MELA-AU 15 42107648 42107648 single base substitution C T exon_variant MELA-AU 15 42107648 42107648 single base substitution C T intron_variant MELA-AU 15 42107648 42107648 single base substitution C T upstream_gene_variant MELA-AU 15 42107688 42107688 single base substitution C T downstream_gene_variant MELA-AU 15 42107688 42107688 single base substitution C T exon_variant MELA-AU 15 42107688 42107688 single base substitution C T intron_variant MELA-AU 15 42107688 42107688 single base substitution C T upstream_gene_variant MELA-AU 15 42108514 42108514 single base substitution T C downstream_gene_variant MELA-AU 15 42108514 42108514 single base substitution T C exon_variant MELA-AU 15 42108514 42108514 single base substitution T C intron_variant MELA-AU 15 42108563 42108563 single base substitution C T downstream_gene_variant MELA-AU 15 42108563 42108563 single base substitution C T exon_variant MELA-AU 15 42108563 42108563 single base substitution C T intron_variant MELA-AU 15 42108669 42108669 single base substitution A T downstream_gene_variant MELA-AU 15 42108669 42108669 single base substitution A T exon_variant MELA-AU 15 42108669 42108669 single base substitution A T intron_variant MELA-AU 15 42108669 42108669 single base substitution A T upstream_gene_variant MELA-AU 15 42108888 42108888 single base substitution C T downstream_gene_variant MELA-AU 15 42108888 42108888 single base substitution C T intron_variant MELA-AU 15 42108888 42108888 single base substitution C T upstream_gene_variant MELA-AU 15 42109095 42109095 single base substitution C T downstream_gene_variant MELA-AU 15 42109095 42109095 single base substitution C T intron_variant MELA-AU 15 42109095 42109095 single base substitution C T upstream_gene_variant MELA-AU 15 42109540 42109540 single base substitution C T downstream_gene_variant MELA-AU 15 42109540 42109540 single base substitution C T intron_variant MELA-AU 15 42109540 42109540 single base substitution C T upstream_gene_variant MELA-AU 15 42109545 42109545 single base substitution G A downstream_gene_variant MELA-AU 15 42109545 42109545 single base substitution G A intron_variant MELA-AU 15 42109545 42109545 single base substitution G A upstream_gene_variant MELA-AU 15 42109967 42109967 single base substitution C T downstream_gene_variant MELA-AU 15 42109967 42109967 single base substitution C T intron_variant MELA-AU 15 42109967 42109967 single base substitution C T upstream_gene_variant MELA-AU 15 42110007 42110007 single base substitution C T downstream_gene_variant MELA-AU 15 42110007 42110007 single base substitution C T intron_variant MELA-AU 15 42110007 42110007 single base substitution C T upstream_gene_variant MELA-AU 15 42110022 42110022 single base substitution C T downstream_gene_variant MELA-AU 15 42110022 42110022 single base substitution C T intron_variant MELA-AU 15 42110022 42110022 single base substitution C T upstream_gene_variant MELA-AU 15 42110523 42110523 single base substitution C T downstream_gene_variant MELA-AU 15 42110523 42110523 single base substitution C T intron_variant MELA-AU 15 42110523 42110523 single base substitution C T upstream_gene_variant MELA-AU 15 42110618 42110618 single base substitution C T downstream_gene_variant MELA-AU 15 42110618 42110618 single base substitution C T intron_variant MELA-AU 15 42110618 42110618 single base substitution C T upstream_gene_variant MELA-AU 15 42111369 42111369 single base substitution C T downstream_gene_variant MELA-AU 15 42111369 42111369 single base substitution C T intron_variant MELA-AU 15 42111369 42111369 single base substitution C T upstream_gene_variant MELA-AU 15 42111397 42111398 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 42111397 42111398 multiple base substitution (>=2bp and <=200bp) CC TT intron_variant MELA-AU 15 42111397 42111398 multiple base substitution (>=2bp and <=200bp) CC TT upstream_gene_variant MELA-AU 15 42111398 42111398 single base substitution C T downstream_gene_variant MELA-AU 15 42111398 42111398 single base substitution C T intron_variant MELA-AU 15 42111398 42111398 single base substitution C T upstream_gene_variant MELA-AU 15 42111550 42111550 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42111550 42111550 single base substitution C T downstream_gene_variant MELA-AU 15 42111550 42111550 single base substitution C T exon_variant MELA-AU 15 42111550 42111550 single base substitution C T missense_variant L639F 1915C>T MELA-AU 15 42111550 42111550 single base substitution C T missense_variant L683F 2047C>T MELA-AU 15 42111550 42111550 single base substitution C T missense_variant L800F 2398C>T MELA-AU 15 42111550 42111550 single base substitution C T missense_variant L806F 2416C>T MELA-AU 15 42111550 42111550 single base substitution C T upstream_gene_variant MELA-AU 15 42111986 42111986 single base substitution C T downstream_gene_variant MELA-AU 15 42111986 42111986 single base substitution C T intron_variant MELA-AU 15 42111986 42111986 single base substitution C T upstream_gene_variant MELA-AU 15 42112504 42112504 single base substitution C T downstream_gene_variant MELA-AU 15 42112504 42112504 single base substitution C T intron_variant MELA-AU 15 42112504 42112504 single base substitution C T upstream_gene_variant MELA-AU 15 42113540 42113540 single base substitution T C downstream_gene_variant MELA-AU 15 42113540 42113540 single base substitution T C intron_variant MELA-AU 15 42113540 42113540 single base substitution T C upstream_gene_variant MELA-AU 15 42113752 42113752 single base substitution C T downstream_gene_variant MELA-AU 15 42113752 42113752 single base substitution C T exon_variant MELA-AU 15 42113752 42113752 single base substitution C T intron_variant MELA-AU 15 42113752 42113752 single base substitution C T upstream_gene_variant MELA-AU 15 42113827 42113827 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42113827 42113827 single base substitution C T downstream_gene_variant MELA-AU 15 42113827 42113827 single base substitution C T exon_variant MELA-AU 15 42113827 42113827 single base substitution C T missense_variant P761S 2281C>T MELA-AU 15 42113827 42113827 single base substitution C T missense_variant P805S 2413C>T MELA-AU 15 42113827 42113827 single base substitution C T missense_variant P922S 2764C>T MELA-AU 15 42113827 42113827 single base substitution C T missense_variant P928S 2782C>T MELA-AU 15 42113827 42113827 single base substitution C T upstream_gene_variant MELA-AU 15 42114169 42114169 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42114169 42114169 single base substitution C T downstream_gene_variant MELA-AU 15 42114169 42114169 single base substitution C T exon_variant MELA-AU 15 42114169 42114169 single base substitution C T synonymous_variant F803F 2409C>T MELA-AU 15 42114169 42114169 single base substitution C T synonymous_variant F847F 2541C>T MELA-AU 15 42114169 42114169 single base substitution C T synonymous_variant F964F 2892C>T MELA-AU 15 42114169 42114169 single base substitution C T synonymous_variant F970F 2910C>T MELA-AU 15 42114169 42114169 single base substitution C T upstream_gene_variant MELA-AU 15 42114972 42114972 single base substitution G A downstream_gene_variant MELA-AU 15 42114972 42114972 single base substitution G A exon_variant MELA-AU 15 42114972 42114972 single base substitution G A intron_variant MELA-AU 15 42115117 42115117 single base substitution C T downstream_gene_variant MELA-AU 15 42115117 42115117 single base substitution C T exon_variant MELA-AU 15 42115117 42115117 single base substitution C T intron_variant MELA-AU 15 42115130 42115130 single base substitution C T downstream_gene_variant MELA-AU 15 42115130 42115130 single base substitution C T exon_variant MELA-AU 15 42115130 42115130 single base substitution C T splice_region_variant MELA-AU 15 42115291 42115291 single base substitution G C 3_prime_UTR_variant MELA-AU 15 42115291 42115291 single base substitution G C downstream_gene_variant MELA-AU 15 42115291 42115291 single base substitution G C exon_variant MELA-AU 15 42115291 42115291 single base substitution G C intron_variant MELA-AU 15 42115291 42115291 single base substitution G C missense_variant A1040P 3118G>C MELA-AU 15 42115291 42115291 single base substitution G C missense_variant A1157P 3469G>C MELA-AU 15 42115291 42115291 single base substitution G C missense_variant A1163P 3487G>C MELA-AU 15 42115291 42115291 single base substitution G C missense_variant A996P 2986G>C MELA-AU 15 42116362 42116362 single base substitution G T downstream_gene_variant MELA-AU 15 42116362 42116362 single base substitution G T intron_variant MELA-AU 15 42116675 42116675 single base substitution C T downstream_gene_variant MELA-AU 15 42116675 42116675 single base substitution C T splice_region_variant MELA-AU 15 42118165 42118165 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42118165 42118165 single base substitution C T downstream_gene_variant MELA-AU 15 42118165 42118165 single base substitution C T exon_variant MELA-AU 15 42118255 42118255 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42118255 42118255 single base substitution C T downstream_gene_variant MELA-AU 15 42118255 42118255 single base substitution C T exon_variant MELA-AU 15 42118264 42118264 single base substitution C T 3_prime_UTR_variant MELA-AU 15 42118264 42118264 single base substitution C T downstream_gene_variant MELA-AU 15 42118264 42118264 single base substitution C T exon_variant MELA-AU 15 42118497 42118497 single base substitution G A 3_prime_UTR_variant MELA-AU 15 42118497 42118497 single base substitution G A downstream_gene_variant MELA-AU 15 42119417 42119417 insertion of <=200bp - TGGAGG 3_prime_UTR_variant MELA-AU 15 42119417 42119417 insertion of <=200bp - TGGAGG downstream_gene_variant MELA-AU 15 42119648 42119649 multiple base substitution (>=2bp and <=200bp) CC TT 3_prime_UTR_variant MELA-AU 15 42119648 42119649 multiple base substitution (>=2bp and <=200bp) CC TT downstream_gene_variant MELA-AU 15 42120261 42120261 single base substitution G A downstream_gene_variant MELA-AU 15 42120395 42120395 single base substitution C T downstream_gene_variant MELA-AU 15 42120816 42120816 single base substitution T G downstream_gene_variant MELA-AU 15 42122383 42122383 single base substitution C T downstream_gene_variant MELA-AU 15 42122398 42122398 single base substitution C T downstream_gene_variant MELA-AU 15 42122933 42122933 single base substitution C T downstream_gene_variant MELA-AU 15 42123331 42123331 single base substitution C T downstream_gene_variant MELA-AU 15 42124425 42124425 single base substitution C T downstream_gene_variant MELA-AU 15 42124744 42124744 single base substitution G A downstream_gene_variant MELA-AU 15 42124840 42124840 single base substitution C T downstream_gene_variant MELA-AU 15 42124845 42124845 single base substitution C T downstream_gene_variant ORCA-IN 15 42081639 42081639 single base substitution C G intron_variant ORCA-IN 15 42105490 42105490 single base substitution C G downstream_gene_variant ORCA-IN 15 42105490 42105490 single base substitution C G exon_variant ORCA-IN 15 42105490 42105490 single base substitution C G intron_variant ORCA-IN 15 42105490 42105490 single base substitution C G upstream_gene_variant OV-AU 15 42062511 42062511 single base substitution G T upstream_gene_variant OV-AU 15 42063631 42063631 single base substitution C G upstream_gene_variant OV-AU 15 42068233 42068233 single base substitution G C intron_variant OV-AU 15 42086566 42086566 single base substitution C A intron_variant OV-AU 15 42102937 42102937 single base substitution A G exon_variant OV-AU 15 42102937 42102937 single base substitution A G intron_variant OV-AU 15 42102937 42102937 single base substitution A G upstream_gene_variant OV-AU 15 42113686 42113686 single base substitution G T downstream_gene_variant OV-AU 15 42113686 42113686 single base substitution G T exon_variant OV-AU 15 42113686 42113686 single base substitution G T intron_variant OV-AU 15 42113686 42113686 single base substitution G T upstream_gene_variant OV-AU 15 42113797 42113797 single base substitution C T 3_prime_UTR_variant OV-AU 15 42113797 42113797 single base substitution C T downstream_gene_variant OV-AU 15 42113797 42113797 single base substitution C T exon_variant OV-AU 15 42113797 42113797 single base substitution C T missense_variant R751W 2251C>T OV-AU 15 42113797 42113797 single base substitution C T missense_variant R795W 2383C>T OV-AU 15 42113797 42113797 single base substitution C T missense_variant R912W 2734C>T OV-AU 15 42113797 42113797 single base substitution C T missense_variant R918W 2752C>T OV-AU 15 42113797 42113797 single base substitution C T upstream_gene_variant OV-AU 15 42117395 42117395 single base substitution G C downstream_gene_variant OV-AU 15 42117395 42117395 single base substitution G C intron_variant PACA-AU 15 42073947 42073947 single base substitution T C intron_variant PACA-AU 15 42074370 42074370 single base substitution G A intron_variant PACA-AU 15 42074579 42074579 single base substitution G T intron_variant PACA-AU 15 42074756 42074756 single base substitution G A intron_variant PACA-AU 15 42078877 42078877 single base substitution G A intron_variant PACA-AU 15 42080893 42080893 single base substitution G A intron_variant PACA-AU 15 42080986 42080986 single base substitution G C intron_variant PACA-AU 15 42081071 42081071 single base substitution G A intron_variant PACA-AU 15 42081400 42081400 single base substitution G C intron_variant PACA-AU 15 42081480 42081480 single base substitution G T intron_variant PACA-AU 15 42081512 42081512 single base substitution A G intron_variant PACA-AU 15 42103029 42103029 single base substitution C T exon_variant PACA-AU 15 42103029 42103029 single base substitution C T intron_variant PACA-AU 15 42107061 42107061 single base substitution C T downstream_gene_variant PACA-AU 15 42107061 42107061 single base substitution C T intron_variant PACA-AU 15 42107061 42107061 single base substitution C T upstream_gene_variant PACA-AU 15 42108559 42108559 single base substitution C G downstream_gene_variant PACA-AU 15 42108559 42108559 single base substitution C G exon_variant PACA-AU 15 42108559 42108559 single base substitution C G intron_variant PACA-AU 15 42110603 42110603 single base substitution C T downstream_gene_variant PACA-AU 15 42110603 42110603 single base substitution C T intron_variant PACA-AU 15 42110603 42110603 single base substitution C T upstream_gene_variant PACA-AU 15 42115558 42115558 single base substitution G A downstream_gene_variant PACA-AU 15 42115558 42115558 single base substitution G A intron_variant PACA-AU 15 42121132 42121132 single base substitution C T downstream_gene_variant PACA-AU 15 42123256 42123256 single base substitution G A downstream_gene_variant PACA-CA 15 42062772 42062772 single base substitution A T upstream_gene_variant PACA-CA 15 42063725 42063725 single base substitution C A upstream_gene_variant PACA-CA 15 42068451 42068451 single base substitution A C intron_variant PACA-CA 15 42073965 42073965 single base substitution C A intron_variant PACA-CA 15 42077906 42077906 deletion of <=200bp A - intron_variant PACA-CA 15 42079469 42079469 single base substitution T C intron_variant PACA-CA 15 42083302 42083302 single base substitution A G intron_variant PACA-CA 15 42083329 42083329 single base substitution A C intron_variant PACA-CA 15 42087058 42087058 single base substitution T C intron_variant PACA-CA 15 42093007 42093007 single base substitution G A intron_variant PACA-CA 15 42093496 42093496 single base substitution A C intron_variant PACA-CA 15 42095755 42095755 insertion of <=200bp - A intron_variant PACA-CA 15 42099819 42099819 single base substitution A C intron_variant PACA-CA 15 42099819 42099819 single base substitution A C upstream_gene_variant PACA-CA 15 42102439 42102439 single base substitution A G intron_variant PACA-CA 15 42102439 42102439 single base substitution A G upstream_gene_variant PACA-CA 15 42103431 42103431 single base substitution G C exon_variant PACA-CA 15 42103431 42103431 single base substitution G C missense_variant E109Q 325G>C PACA-CA 15 42103431 42103431 single base substitution G C splice_region_variant PACA-CA 15 42104353 42104353 single base substitution A G downstream_gene_variant PACA-CA 15 42104353 42104353 single base substitution A G intron_variant PACA-CA 15 42104353 42104353 single base substitution A G upstream_gene_variant PACA-CA 15 42104459 42104459 single base substitution A G downstream_gene_variant PACA-CA 15 42104459 42104459 single base substitution A G intron_variant PACA-CA 15 42104459 42104459 single base substitution A G upstream_gene_variant PACA-CA 15 42105270 42105270 single base substitution A C 3_prime_UTR_variant PACA-CA 15 42105270 42105270 single base substitution A C downstream_gene_variant PACA-CA 15 42105270 42105270 single base substitution A C exon_variant PACA-CA 15 42105270 42105270 single base substitution A C synonymous_variant R152R 454A>C PACA-CA 15 42105270 42105270 single base substitution A C synonymous_variant R264R 790A>C PACA-CA 15 42105270 42105270 single base substitution A C upstream_gene_variant PACA-CA 15 42113653 42113653 single base substitution C G downstream_gene_variant PACA-CA 15 42113653 42113653 single base substitution C G exon_variant PACA-CA 15 42113653 42113653 single base substitution C G intron_variant PACA-CA 15 42113653 42113653 single base substitution C G upstream_gene_variant PACA-CA 15 42114457 42114457 single base substitution C T 3_prime_UTR_variant PACA-CA 15 42114457 42114457 single base substitution C T exon_variant PACA-CA 15 42114457 42114457 single base substitution C T synonymous_variant G1022G 3066C>T PACA-CA 15 42114457 42114457 single base substitution C T synonymous_variant G1028G 3084C>T PACA-CA 15 42114457 42114457 single base substitution C T synonymous_variant G861G 2583C>T PACA-CA 15 42114457 42114457 single base substitution C T synonymous_variant G905G 2715C>T PACA-CA 15 42114457 42114457 single base substitution C T upstream_gene_variant PACA-CA 15 42115319 42115319 single base substitution G A 3_prime_UTR_variant PACA-CA 15 42115319 42115319 single base substitution G A downstream_gene_variant PACA-CA 15 42115319 42115319 single base substitution G A exon_variant PACA-CA 15 42115319 42115319 single base substitution G A intron_variant PACA-CA 15 42115319 42115319 single base substitution G A missense_variant R1005H 3014G>A PACA-CA 15 42115319 42115319 single base substitution G A missense_variant R1049H 3146G>A PACA-CA 15 42115319 42115319 single base substitution G A missense_variant R1166H 3497G>A PACA-CA 15 42115319 42115319 single base substitution G A missense_variant R1172H 3515G>A PACA-CA 15 42121038 42121038 single base substitution T C downstream_gene_variant PAEN-AU 15 42091180 42091180 single base substitution G T intron_variant PAEN-IT 15 42064694 42064694 single base substitution G A upstream_gene_variant PAEN-IT 15 42083264 42083264 single base substitution G T intron_variant PAEN-IT 15 42098468 42098468 single base substitution T C intron_variant PAEN-IT 15 42098468 42098468 single base substitution T C upstream_gene_variant PBCA-DE 15 42089798 42089798 single base substitution G T intron_variant PBCA-DE 15 42096591 42096591 single base substitution A G intron_variant PRAD-CA 15 42123442 42123442 single base substitution G A downstream_gene_variant PRAD-UK 15 42065238 42065238 single base substitution C T upstream_gene_variant PRAD-UK 15 42065857 42065857 single base substitution A G upstream_gene_variant PRAD-UK 15 42091446 42091446 single base substitution T G intron_variant PRAD-UK 15 42114404 42114404 single base substitution C T intron_variant PRAD-UK 15 42114404 42114404 single base substitution C T upstream_gene_variant PRAD-US 15 42105829 42105829 single base substitution C A 3_prime_UTR_variant PRAD-US 15 42105829 42105829 single base substitution C A downstream_gene_variant PRAD-US 15 42105829 42105829 single base substitution C A exon_variant PRAD-US 15 42105829 42105829 single base substitution C A intron_variant PRAD-US 15 42105829 42105829 single base substitution C A missense_variant A165D 494C>A PRAD-US 15 42105829 42105829 single base substitution C A missense_variant A277D 830C>A PRAD-US 15 42105829 42105829 single base substitution C A missense_variant A283D 848C>A PRAD-US 15 42105829 42105829 single base substitution C A upstream_gene_variant RECA-EU 15 42084448 42084448 single base substitution C T intron_variant RECA-EU 15 42088123 42088123 single base substitution A T intron_variant RECA-EU 15 42088804 42088804 single base substitution C T intron_variant RECA-EU 15 42089223 42089223 single base substitution G C intron_variant RECA-EU 15 42089224 42089224 single base substitution C T intron_variant RECA-EU 15 42112021 42112021 single base substitution G T downstream_gene_variant RECA-EU 15 42112021 42112021 single base substitution G T intron_variant RECA-EU 15 42112021 42112021 single base substitution G T upstream_gene_variant RECA-EU 15 42112022 42112022 single base substitution G T downstream_gene_variant RECA-EU 15 42112022 42112022 single base substitution G T intron_variant RECA-EU 15 42112022 42112022 single base substitution G T upstream_gene_variant RECA-EU 15 42113257 42113257 single base substitution C T 3_prime_UTR_variant RECA-EU 15 42113257 42113257 single base substitution C T downstream_gene_variant RECA-EU 15 42113257 42113257 single base substitution C T exon_variant RECA-EU 15 42113257 42113257 single base substitution C T synonymous_variant L742L 2226C>T RECA-EU 15 42113257 42113257 single base substitution C T synonymous_variant L786L 2358C>T RECA-EU 15 42113257 42113257 single base substitution C T synonymous_variant L903L 2709C>T RECA-EU 15 42113257 42113257 single base substitution C T synonymous_variant L909L 2727C>T RECA-EU 15 42113257 42113257 single base substitution C T upstream_gene_variant SKCA-BR 15 42065493 42065493 single base substitution C T upstream_gene_variant SKCA-BR 15 42065752 42065752 single base substitution A G upstream_gene_variant SKCA-BR 15 42073597 42073597 insertion of <=200bp - GT intron_variant SKCA-BR 15 42076756 42076756 single base substitution T G intron_variant SKCA-BR 15 42078975 42078975 insertion of <=200bp - AAATATATATATATATATATAT intron_variant SKCA-BR 15 42078977 42078977 single base substitution T A intron_variant SKCA-BR 15 42078980 42078981 deletion of <=200bp AT - intron_variant SKCA-BR 15 42090807 42090807 single base substitution G A intron_variant SKCA-BR 15 42091838 42091838 single base substitution C T intron_variant SKCA-BR 15 42093985 42093985 single base substitution T G intron_variant SKCA-BR 15 42094156 42094156 single base substitution C T intron_variant SKCA-BR 15 42102741 42102743 deletion of <=200bp CAA - intron_variant SKCA-BR 15 42102741 42102743 deletion of <=200bp CAA - upstream_gene_variant SKCA-BR 15 42103822 42103822 single base substitution C T downstream_gene_variant SKCA-BR 15 42103822 42103822 single base substitution C T exon_variant SKCA-BR 15 42103822 42103822 single base substitution C T intron_variant SKCA-BR 15 42103822 42103822 single base substitution C T upstream_gene_variant SKCA-BR 15 42104339 42104339 single base substitution T G downstream_gene_variant SKCA-BR 15 42104339 42104339 single base substitution T G intron_variant SKCA-BR 15 42104339 42104339 single base substitution T G upstream_gene_variant SKCA-BR 15 42105412 42105412 single base substitution G A downstream_gene_variant SKCA-BR 15 42105412 42105412 single base substitution G A exon_variant SKCA-BR 15 42105412 42105412 single base substitution G A intron_variant SKCA-BR 15 42105412 42105412 single base substitution G A upstream_gene_variant SKCA-BR 15 42107609 42107609 single base substitution C T downstream_gene_variant SKCA-BR 15 42107609 42107609 single base substitution C T exon_variant SKCA-BR 15 42107609 42107609 single base substitution C T intron_variant SKCA-BR 15 42107609 42107609 single base substitution C T splice_region_variant SKCA-BR 15 42107609 42107609 single base substitution C T upstream_gene_variant SKCA-BR 15 42107687 42107687 single base substitution C T downstream_gene_variant SKCA-BR 15 42107687 42107687 single base substitution C T exon_variant SKCA-BR 15 42107687 42107687 single base substitution C T intron_variant SKCA-BR 15 42107687 42107687 single base substitution C T upstream_gene_variant SKCA-BR 15 42109692 42109692 single base substitution A G downstream_gene_variant SKCA-BR 15 42109692 42109692 single base substitution A G intron_variant SKCA-BR 15 42109692 42109692 single base substitution A G upstream_gene_variant SKCA-BR 15 42109696 42109696 single base substitution C G downstream_gene_variant SKCA-BR 15 42109696 42109696 single base substitution C G intron_variant SKCA-BR 15 42109696 42109696 single base substitution C G upstream_gene_variant SKCA-BR 15 42109701 42109701 single base substitution T G downstream_gene_variant SKCA-BR 15 42109701 42109701 single base substitution T G intron_variant SKCA-BR 15 42109701 42109701 single base substitution T G upstream_gene_variant SKCA-BR 15 42110954 42110954 single base substitution A G downstream_gene_variant SKCA-BR 15 42110954 42110954 single base substitution A G intron_variant SKCA-BR 15 42110954 42110954 single base substitution A G upstream_gene_variant SKCA-BR 15 42113838 42113838 single base substitution C T 3_prime_UTR_variant SKCA-BR 15 42113838 42113838 single base substitution C T downstream_gene_variant SKCA-BR 15 42113838 42113838 single base substitution C T exon_variant SKCA-BR 15 42113838 42113838 single base substitution C T synonymous_variant I764I 2292C>T SKCA-BR 15 42113838 42113838 single base substitution C T synonymous_variant I808I 2424C>T SKCA-BR 15 42113838 42113838 single base substitution C T synonymous_variant I925I 2775C>T SKCA-BR 15 42113838 42113838 single base substitution C T synonymous_variant I931I 2793C>T SKCA-BR 15 42113838 42113838 single base substitution C T upstream_gene_variant SKCA-BR 15 42114054 42114054 single base substitution C T downstream_gene_variant SKCA-BR 15 42114054 42114054 single base substitution C T intron_variant SKCA-BR 15 42114054 42114054 single base substitution C T upstream_gene_variant SKCA-BR 15 42119371 42119402 deletion of <=200bp AATCCCAGCTACTCGGGAGGTTTAGGCAGGAG - 3_prime_UTR_variant SKCA-BR 15 42119371 42119402 deletion of <=200bp AATCCCAGCTACTCGGGAGGTTTAGGCAGGAG - downstream_gene_variant SKCA-BR 15 42122672 42122672 single base substitution A G downstream_gene_variant SKCA-BR 15 42124840 42124840 single base substitution C T downstream_gene_variant SKCM-US 15 42067532 42067532 single base substitution C T 5_prime_UTR_variant SKCM-US 15 42067532 42067532 single base substitution C T exon_variant SKCM-US 15 42067532 42067532 single base substitution C T missense_variant S20F 59C>T SKCM-US 15 42067532 42067532 single base substitution C T upstream_gene_variant SKCM-US 15 42104844 42104844 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42104844 42104844 single base substitution C T downstream_gene_variant SKCM-US 15 42104844 42104844 single base substitution C T exon_variant SKCM-US 15 42104844 42104844 single base substitution C T missense_variant T210I 629C>T SKCM-US 15 42104844 42104844 single base substitution C T missense_variant T98I 293C>T SKCM-US 15 42104844 42104844 single base substitution C T upstream_gene_variant SKCM-US 15 42105143 42105143 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42105143 42105143 single base substitution C T downstream_gene_variant SKCM-US 15 42105143 42105143 single base substitution C T exon_variant SKCM-US 15 42105143 42105143 single base substitution C T synonymous_variant G109G 327C>T SKCM-US 15 42105143 42105143 single base substitution C T synonymous_variant G221G 663C>T SKCM-US 15 42105143 42105143 single base substitution C T upstream_gene_variant SKCM-US 15 42105202 42105202 single base substitution G A 3_prime_UTR_variant SKCM-US 15 42105202 42105202 single base substitution G A downstream_gene_variant SKCM-US 15 42105202 42105202 single base substitution G A exon_variant SKCM-US 15 42105202 42105202 single base substitution G A missense_variant R129K 386G>A SKCM-US 15 42105202 42105202 single base substitution G A missense_variant R241K 722G>A SKCM-US 15 42105202 42105202 single base substitution G A upstream_gene_variant SKCM-US 15 42105899 42105899 single base substitution C G 3_prime_UTR_variant SKCM-US 15 42105899 42105899 single base substitution C G downstream_gene_variant SKCM-US 15 42105899 42105899 single base substitution C G exon_variant SKCM-US 15 42105899 42105899 single base substitution C G intron_variant SKCM-US 15 42105899 42105899 single base substitution C G missense_variant N188K 564C>G SKCM-US 15 42105899 42105899 single base substitution C G missense_variant N300K 900C>G SKCM-US 15 42105899 42105899 single base substitution C G missense_variant N306K 918C>G SKCM-US 15 42105899 42105899 single base substitution C G upstream_gene_variant SKCM-US 15 42107506 42107506 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42107506 42107506 single base substitution C T downstream_gene_variant SKCM-US 15 42107506 42107506 single base substitution C T exon_variant SKCM-US 15 42107506 42107506 single base substitution C T intron_variant SKCM-US 15 42107506 42107506 single base substitution C T missense_variant S290F 869C>T SKCM-US 15 42107506 42107506 single base substitution C T missense_variant S407F 1220C>T SKCM-US 15 42107506 42107506 single base substitution C T missense_variant S413F 1238C>T SKCM-US 15 42107506 42107506 single base substitution C T upstream_gene_variant SKCM-US 15 42107533 42107533 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42107533 42107533 single base substitution C T downstream_gene_variant SKCM-US 15 42107533 42107533 single base substitution C T exon_variant SKCM-US 15 42107533 42107533 single base substitution C T intron_variant SKCM-US 15 42107533 42107533 single base substitution C T missense_variant T299I 896C>T SKCM-US 15 42107533 42107533 single base substitution C T missense_variant T416I 1247C>T SKCM-US 15 42107533 42107533 single base substitution C T missense_variant T422I 1265C>T SKCM-US 15 42107533 42107533 single base substitution C T upstream_gene_variant SKCM-US 15 42107932 42107932 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42107932 42107932 single base substitution C T downstream_gene_variant SKCM-US 15 42107932 42107932 single base substitution C T exon_variant SKCM-US 15 42107932 42107932 single base substitution C T synonymous_variant I315I 945C>T SKCM-US 15 42107932 42107932 single base substitution C T synonymous_variant I359I 1077C>T SKCM-US 15 42107932 42107932 single base substitution C T synonymous_variant I476I 1428C>T SKCM-US 15 42107932 42107932 single base substitution C T synonymous_variant I482I 1446C>T SKCM-US 15 42107932 42107932 single base substitution C T upstream_gene_variant SKCM-US 15 42109904 42109904 single base substitution G A 3_prime_UTR_variant SKCM-US 15 42109904 42109904 single base substitution G A downstream_gene_variant SKCM-US 15 42109904 42109904 single base substitution G A exon_variant SKCM-US 15 42109904 42109904 single base substitution G A synonymous_variant T464T 1392G>A SKCM-US 15 42109904 42109904 single base substitution G A synonymous_variant T508T 1524G>A SKCM-US 15 42109904 42109904 single base substitution G A synonymous_variant T625T 1875G>A SKCM-US 15 42109904 42109904 single base substitution G A synonymous_variant T631T 1893G>A SKCM-US 15 42109904 42109904 single base substitution G A upstream_gene_variant SKCM-US 15 42109932 42109932 single base substitution C T downstream_gene_variant SKCM-US 15 42109932 42109932 single base substitution C T missense_variant R474W 1420C>T SKCM-US 15 42109932 42109932 single base substitution C T missense_variant R518W 1552C>T SKCM-US 15 42109932 42109932 single base substitution C T missense_variant R635W 1903C>T SKCM-US 15 42109932 42109932 single base substitution C T missense_variant R641W 1921C>T SKCM-US 15 42109932 42109932 single base substitution C T splice_region_variant SKCM-US 15 42109932 42109932 single base substitution C T upstream_gene_variant SKCM-US 15 42110405 42110405 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42110405 42110405 single base substitution C T downstream_gene_variant SKCM-US 15 42110405 42110405 single base substitution C T exon_variant SKCM-US 15 42110405 42110405 single base substitution C T missense_variant P504L 1511C>T SKCM-US 15 42110405 42110405 single base substitution C T missense_variant P548L 1643C>T SKCM-US 15 42110405 42110405 single base substitution C T missense_variant P665L 1994C>T SKCM-US 15 42110405 42110405 single base substitution C T missense_variant P671L 2012C>T SKCM-US 15 42110405 42110405 single base substitution C T upstream_gene_variant SKCM-US 15 42111090 42111090 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42111090 42111090 single base substitution C T downstream_gene_variant SKCM-US 15 42111090 42111090 single base substitution C T exon_variant SKCM-US 15 42111090 42111090 single base substitution C T synonymous_variant R581R 1743C>T SKCM-US 15 42111090 42111090 single base substitution C T synonymous_variant R625R 1875C>T SKCM-US 15 42111090 42111090 single base substitution C T synonymous_variant R742R 2226C>T SKCM-US 15 42111090 42111090 single base substitution C T synonymous_variant R748R 2244C>T SKCM-US 15 42111090 42111090 single base substitution C T upstream_gene_variant SKCM-US 15 42111098 42111098 single base substitution A G 3_prime_UTR_variant SKCM-US 15 42111098 42111098 single base substitution A G downstream_gene_variant SKCM-US 15 42111098 42111098 single base substitution A G exon_variant SKCM-US 15 42111098 42111098 single base substitution A G missense_variant Q584R 1751A>G SKCM-US 15 42111098 42111098 single base substitution A G missense_variant Q628R 1883A>G SKCM-US 15 42111098 42111098 single base substitution A G missense_variant Q745R 2234A>G SKCM-US 15 42111098 42111098 single base substitution A G missense_variant Q751R 2252A>G SKCM-US 15 42111098 42111098 single base substitution A G upstream_gene_variant SKCM-US 15 42111801 42111801 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42111801 42111801 single base substitution C T downstream_gene_variant SKCM-US 15 42111801 42111801 single base substitution C T exon_variant SKCM-US 15 42111801 42111801 single base substitution C T missense_variant P651S 1951C>T SKCM-US 15 42111801 42111801 single base substitution C T missense_variant P695S 2083C>T SKCM-US 15 42111801 42111801 single base substitution C T missense_variant P812S 2434C>T SKCM-US 15 42111801 42111801 single base substitution C T missense_variant P818S 2452C>T SKCM-US 15 42111801 42111801 single base substitution C T upstream_gene_variant SKCM-US 15 42113041 42113041 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42113041 42113041 single base substitution C T downstream_gene_variant SKCM-US 15 42113041 42113041 single base substitution C T exon_variant SKCM-US 15 42113041 42113041 single base substitution C T synonymous_variant S670S 2010C>T SKCM-US 15 42113041 42113041 single base substitution C T synonymous_variant S714S 2142C>T SKCM-US 15 42113041 42113041 single base substitution C T synonymous_variant S831S 2493C>T SKCM-US 15 42113041 42113041 single base substitution C T synonymous_variant S837S 2511C>T SKCM-US 15 42113041 42113041 single base substitution C T upstream_gene_variant SKCM-US 15 42113243 42113243 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42113243 42113243 single base substitution C T downstream_gene_variant SKCM-US 15 42113243 42113243 single base substitution C T exon_variant SKCM-US 15 42113243 42113243 single base substitution C T missense_variant L738F 2212C>T SKCM-US 15 42113243 42113243 single base substitution C T missense_variant L782F 2344C>T SKCM-US 15 42113243 42113243 single base substitution C T missense_variant L899F 2695C>T SKCM-US 15 42113243 42113243 single base substitution C T missense_variant L905F 2713C>T SKCM-US 15 42113243 42113243 single base substitution C T upstream_gene_variant SKCM-US 15 42113890 42113890 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42113890 42113890 single base substitution C T downstream_gene_variant SKCM-US 15 42113890 42113890 single base substitution C T exon_variant SKCM-US 15 42113890 42113890 single base substitution C T missense_variant P782S 2344C>T SKCM-US 15 42113890 42113890 single base substitution C T missense_variant P826S 2476C>T SKCM-US 15 42113890 42113890 single base substitution C T missense_variant P943S 2827C>T SKCM-US 15 42113890 42113890 single base substitution C T missense_variant P949S 2845C>T SKCM-US 15 42113890 42113890 single base substitution C T upstream_gene_variant SKCM-US 15 42114441 42114441 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42114441 42114441 single base substitution C T exon_variant SKCM-US 15 42114441 42114441 single base substitution C T missense_variant P1017L 3050C>T SKCM-US 15 42114441 42114441 single base substitution C T missense_variant P1023L 3068C>T SKCM-US 15 42114441 42114441 single base substitution C T missense_variant P856L 2567C>T SKCM-US 15 42114441 42114441 single base substitution C T missense_variant P900L 2699C>T SKCM-US 15 42114441 42114441 single base substitution C T upstream_gene_variant SKCM-US 15 42115750 42115750 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42115750 42115750 single base substitution C T downstream_gene_variant SKCM-US 15 42115750 42115750 single base substitution C T exon_variant SKCM-US 15 42115750 42115750 single base substitution C T intron_variant SKCM-US 15 42115750 42115750 single base substitution C T missense_variant P1074L 3221C>T SKCM-US 15 42115750 42115750 single base substitution C T missense_variant P1118L 3353C>T SKCM-US 15 42115750 42115750 single base substitution C T missense_variant P1235L 3704C>T SKCM-US 15 42115750 42115750 single base substitution C T missense_variant P1241L 3722C>T SKCM-US 15 42116018 42116018 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42116018 42116018 single base substitution C T downstream_gene_variant SKCM-US 15 42116018 42116018 single base substitution C T exon_variant SKCM-US 15 42116018 42116018 single base substitution C T intron_variant SKCM-US 15 42116018 42116018 single base substitution C T synonymous_variant F1163F 3489C>T SKCM-US 15 42116018 42116018 single base substitution C T synonymous_variant F1207F 3621C>T SKCM-US 15 42116018 42116018 single base substitution C T synonymous_variant F1324F 3972C>T SKCM-US 15 42116018 42116018 single base substitution C T synonymous_variant F1330F 3990C>T SKCM-US 15 42116019 42116019 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42116019 42116019 single base substitution C T downstream_gene_variant SKCM-US 15 42116019 42116019 single base substitution C T exon_variant SKCM-US 15 42116019 42116019 single base substitution C T intron_variant SKCM-US 15 42116019 42116019 single base substitution C T missense_variant P1164S 3490C>T SKCM-US 15 42116019 42116019 single base substitution C T missense_variant P1208S 3622C>T SKCM-US 15 42116019 42116019 single base substitution C T missense_variant P1325S 3973C>T SKCM-US 15 42116019 42116019 single base substitution C T missense_variant P1331S 3991C>T SKCM-US 15 42116122 42116122 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42116122 42116122 single base substitution C T downstream_gene_variant SKCM-US 15 42116122 42116122 single base substitution C T exon_variant SKCM-US 15 42116122 42116122 single base substitution C T intron_variant SKCM-US 15 42116122 42116122 single base substitution C T missense_variant P1198L 3593C>T SKCM-US 15 42116122 42116122 single base substitution C T missense_variant P1242L 3725C>T SKCM-US 15 42116122 42116122 single base substitution C T missense_variant P1359L 4076C>T SKCM-US 15 42116122 42116122 single base substitution C T missense_variant P1365L 4094C>T SKCM-US 15 42116130 42116130 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42116130 42116130 single base substitution C T downstream_gene_variant SKCM-US 15 42116130 42116130 single base substitution C T exon_variant SKCM-US 15 42116130 42116130 single base substitution C T intron_variant SKCM-US 15 42116130 42116130 single base substitution C T missense_variant P1201S 3601C>T SKCM-US 15 42116130 42116130 single base substitution C T missense_variant P1245S 3733C>T SKCM-US 15 42116130 42116130 single base substitution C T missense_variant P1362S 4084C>T SKCM-US 15 42116130 42116130 single base substitution C T missense_variant P1368S 4102C>T SKCM-US 15 42117477 42117477 single base substitution C T 3_prime_UTR_variant SKCM-US 15 42117477 42117477 single base substitution C T downstream_gene_variant SKCM-US 15 42117477 42117477 single base substitution C T exon_variant SKCM-US 15 42117477 42117477 single base substitution C T missense_variant S1180L 3539C>T SKCM-US 15 42117477 42117477 single base substitution C T missense_variant S1296L 3887C>T SKCM-US 15 42117477 42117477 single base substitution C T missense_variant S1340L 4019C>T SKCM-US 15 42117477 42117477 single base substitution C T missense_variant S1457L 4370C>T SKCM-US 15 42117477 42117477 single base substitution C T missense_variant S1463L 4388C>T STAD-US 15 42067510 42067510 single base substitution A G 5_prime_UTR_variant STAD-US 15 42067510 42067510 single base substitution A G exon_variant STAD-US 15 42067510 42067510 single base substitution A G missense_variant K13E 37A>G STAD-US 15 42067510 42067510 single base substitution A G upstream_gene_variant STAD-US 15 42105142 42105142 single base substitution G A 3_prime_UTR_variant STAD-US 15 42105142 42105142 single base substitution G A downstream_gene_variant STAD-US 15 42105142 42105142 single base substitution G A exon_variant STAD-US 15 42105142 42105142 single base substitution G A missense_variant G109D 326G>A STAD-US 15 42105142 42105142 single base substitution G A missense_variant G221D 662G>A STAD-US 15 42105142 42105142 single base substitution G A upstream_gene_variant STAD-US 15 42105153 42105153 single base substitution C T 3_prime_UTR_variant STAD-US 15 42105153 42105153 single base substitution C T downstream_gene_variant STAD-US 15 42105153 42105153 single base substitution C T exon_variant STAD-US 15 42105153 42105153 single base substitution C T synonymous_variant L113L 337C>T STAD-US 15 42105153 42105153 single base substitution C T synonymous_variant L225L 673C>T STAD-US 15 42105153 42105153 single base substitution C T upstream_gene_variant STAD-US 15 42105236 42105236 single base substitution G A 3_prime_UTR_variant STAD-US 15 42105236 42105236 single base substitution G A downstream_gene_variant STAD-US 15 42105236 42105236 single base substitution G A exon_variant STAD-US 15 42105236 42105236 single base substitution G A synonymous_variant T140T 420G>A STAD-US 15 42105236 42105236 single base substitution G A synonymous_variant T252T 756G>A STAD-US 15 42105236 42105236 single base substitution G A upstream_gene_variant STAD-US 15 42105237 42105237 single base substitution T A 3_prime_UTR_variant STAD-US 15 42105237 42105237 single base substitution T A downstream_gene_variant STAD-US 15 42105237 42105237 single base substitution T A exon_variant STAD-US 15 42105237 42105237 single base substitution T A missense_variant S141T 421T>A STAD-US 15 42105237 42105237 single base substitution T A missense_variant S253T 757T>A STAD-US 15 42105237 42105237 single base substitution T A upstream_gene_variant STAD-US 15 42106789 42106789 single base substitution C T 3_prime_UTR_variant STAD-US 15 42106789 42106789 single base substitution C T downstream_gene_variant STAD-US 15 42106789 42106789 single base substitution C T exon_variant STAD-US 15 42106789 42106789 single base substitution C T intron_variant STAD-US 15 42106789 42106789 single base substitution C T missense_variant T229I 686C>T STAD-US 15 42106789 42106789 single base substitution C T missense_variant T341I 1022C>T STAD-US 15 42106789 42106789 single base substitution C T missense_variant T347I 1040C>T STAD-US 15 42106789 42106789 single base substitution C T upstream_gene_variant STAD-US 15 42109622 42109622 single base substitution C T 3_prime_UTR_variant STAD-US 15 42109622 42109622 single base substitution C T downstream_gene_variant STAD-US 15 42109622 42109622 single base substitution C T exon_variant STAD-US 15 42109622 42109622 single base substitution C T missense_variant A422V 1265C>T STAD-US 15 42109622 42109622 single base substitution C T missense_variant A466V 1397C>T STAD-US 15 42109622 42109622 single base substitution C T missense_variant A583V 1748C>T STAD-US 15 42109622 42109622 single base substitution C T missense_variant A589V 1766C>T STAD-US 15 42109622 42109622 single base substitution C T upstream_gene_variant STAD-US 15 42109837 42109837 single base substitution G A 3_prime_UTR_variant STAD-US 15 42109837 42109837 single base substitution G A downstream_gene_variant STAD-US 15 42109837 42109837 single base substitution G A exon_variant STAD-US 15 42109837 42109837 single base substitution G A missense_variant R442Q 1325G>A STAD-US 15 42109837 42109837 single base substitution G A missense_variant R486Q 1457G>A STAD-US 15 42109837 42109837 single base substitution G A missense_variant R603Q 1808G>A STAD-US 15 42109837 42109837 single base substitution G A missense_variant R609Q 1826G>A STAD-US 15 42109837 42109837 single base substitution G A upstream_gene_variant STAD-US 15 42110261 42110261 single base substitution T C 3_prime_UTR_variant STAD-US 15 42110261 42110261 single base substitution T C downstream_gene_variant STAD-US 15 42110261 42110261 single base substitution T C exon_variant STAD-US 15 42110261 42110261 single base substitution T C synonymous_variant G492G 1476T>C STAD-US 15 42110261 42110261 single base substitution T C synonymous_variant G536G 1608T>C STAD-US 15 42110261 42110261 single base substitution T C synonymous_variant G653G 1959T>C STAD-US 15 42110261 42110261 single base substitution T C synonymous_variant G659G 1977T>C STAD-US 15 42110261 42110261 single base substitution T C upstream_gene_variant STAD-US 15 42110453 42110453 deletion of <=200bp T - 3_prime_UTR_variant STAD-US 15 42110453 42110453 deletion of <=200bp T - downstream_gene_variant STAD-US 15 42110453 42110453 deletion of <=200bp T - exon_variant STAD-US 15 42110453 42110453 deletion of <=200bp T - frameshift_variant I520 STAD-US 15 42110453 42110453 deletion of <=200bp T - frameshift_variant I564 STAD-US 15 42110453 42110453 deletion of <=200bp T - frameshift_variant I681 STAD-US 15 42110453 42110453 deletion of <=200bp T - frameshift_variant I687 STAD-US 15 42110453 42110453 deletion of <=200bp T - upstream_gene_variant STAD-US 15 42111038 42111038 single base substitution G A 3_prime_UTR_variant STAD-US 15 42111038 42111038 single base substitution G A downstream_gene_variant STAD-US 15 42111038 42111038 single base substitution G A exon_variant STAD-US 15 42111038 42111038 single base substitution G A missense_variant R564H 1691G>A STAD-US 15 42111038 42111038 single base substitution G A missense_variant R608H 1823G>A STAD-US 15 42111038 42111038 single base substitution G A missense_variant R725H 2174G>A STAD-US 15 42111038 42111038 single base substitution G A missense_variant R731H 2192G>A STAD-US 15 42111038 42111038 single base substitution G A upstream_gene_variant STAD-US 15 42111819 42111819 single base substitution C T 3_prime_UTR_variant STAD-US 15 42111819 42111819 single base substitution C T downstream_gene_variant STAD-US 15 42111819 42111819 single base substitution C T exon_variant STAD-US 15 42111819 42111819 single base substitution C T stop_gained R657* 1969C>T STAD-US 15 42111819 42111819 single base substitution C T stop_gained R701* 2101C>T STAD-US 15 42111819 42111819 single base substitution C T stop_gained R818* 2452C>T STAD-US 15 42111819 42111819 single base substitution C T stop_gained R824* 2470C>T STAD-US 15 42111819 42111819 single base substitution C T upstream_gene_variant STAD-US 15 42115796 42115796 single base substitution C A 3_prime_UTR_variant STAD-US 15 42115796 42115796 single base substitution C A downstream_gene_variant STAD-US 15 42115796 42115796 single base substitution C A exon_variant STAD-US 15 42115796 42115796 single base substitution C A intron_variant STAD-US 15 42115796 42115796 single base substitution C A synonymous_variant A1089A 3267C>A STAD-US 15 42115796 42115796 single base substitution C A synonymous_variant A1133A 3399C>A STAD-US 15 42115796 42115796 single base substitution C A synonymous_variant A1250A 3750C>A STAD-US 15 42115796 42115796 single base substitution C A synonymous_variant A1256A 3768C>A STAD-US 15 42116010 42116010 single base substitution C T 3_prime_UTR_variant STAD-US 15 42116010 42116010 single base substitution C T downstream_gene_variant STAD-US 15 42116010 42116010 single base substitution C T exon_variant STAD-US 15 42116010 42116010 single base substitution C T intron_variant STAD-US 15 42116010 42116010 single base substitution C T missense_variant P1161S 3481C>T STAD-US 15 42116010 42116010 single base substitution C T missense_variant P1205S 3613C>T STAD-US 15 42116010 42116010 single base substitution C T missense_variant P1322S 3964C>T STAD-US 15 42116010 42116010 single base substitution C T missense_variant P1328S 3982C>T STAD-US 15 42116181 42116181 single base substitution T C 3_prime_UTR_variant STAD-US 15 42116181 42116181 single base substitution T C downstream_gene_variant STAD-US 15 42116181 42116181 single base substitution T C exon_variant STAD-US 15 42116181 42116181 single base substitution T C intron_variant STAD-US 15 42116181 42116181 single base substitution T C synonymous_variant L1218L 3652T>C STAD-US 15 42116181 42116181 single base substitution T C synonymous_variant L1262L 3784T>C STAD-US 15 42116181 42116181 single base substitution T C synonymous_variant L1379L 4135T>C STAD-US 15 42116181 42116181 single base substitution T C synonymous_variant L1385L 4153T>C THCA-SA 15 42109223 42109223 single base substitution T C 3_prime_UTR_variant THCA-SA 15 42109223 42109223 single base substitution T C downstream_gene_variant THCA-SA 15 42109223 42109223 single base substitution T C exon_variant THCA-SA 15 42109223 42109223 single base substitution T C synonymous_variant V406V 1218T>C THCA-SA 15 42109223 42109223 single base substitution T C synonymous_variant V450V 1350T>C THCA-SA 15 42109223 42109223 single base substitution T C synonymous_variant V567V 1701T>C THCA-SA 15 42109223 42109223 single base substitution T C synonymous_variant V573V 1719T>C THCA-SA 15 42109223 42109223 single base substitution T C upstream_gene_variant THCA-SA 15 42115381 42115381 single base substitution C T 3_prime_UTR_variant THCA-SA 15 42115381 42115381 single base substitution C T downstream_gene_variant THCA-SA 15 42115381 42115381 single base substitution C T exon_variant THCA-SA 15 42115381 42115381 single base substitution C T intron_variant THCA-SA 15 42115381 42115381 single base substitution C T missense_variant L1026F 3076C>T THCA-SA 15 42115381 42115381 single base substitution C T missense_variant L1070F 3208C>T THCA-SA 15 42115381 42115381 single base substitution C T missense_variant L1187F 3559C>T THCA-SA 15 42115381 42115381 single base substitution C T missense_variant L1193F 3577C>T THCA-SA 15 42115747 42115747 single base substitution G C 3_prime_UTR_variant THCA-SA 15 42115747 42115747 single base substitution G C downstream_gene_variant THCA-SA 15 42115747 42115747 single base substitution G C exon_variant THCA-SA 15 42115747 42115747 single base substitution G C intron_variant THCA-SA 15 42115747 42115747 single base substitution G C missense_variant R1073P 3218G>C THCA-SA 15 42115747 42115747 single base substitution G C missense_variant R1117P 3350G>C THCA-SA 15 42115747 42115747 single base substitution G C missense_variant R1234P 3701G>C THCA-SA 15 42115747 42115747 single base substitution G C missense_variant R1240P 3719G>C THCA-SA 15 42118123 42118123 single base substitution G C 3_prime_UTR_variant THCA-SA 15 42118123 42118123 single base substitution G C downstream_gene_variant THCA-SA 15 42118123 42118123 single base substitution G C exon_variant THCA-SA 15 42118651 42118651 single base substitution T C 3_prime_UTR_variant THCA-SA 15 42118651 42118651 single base substitution T C downstream_gene_variant THCA-SA 15 42118971 42118971 single base substitution A G 3_prime_UTR_variant THCA-SA 15 42118971 42118971 single base substitution A G downstream_gene_variant THCA-SA 15 42119593 42119593 single base substitution C A 3_prime_UTR_variant THCA-SA 15 42119593 42119593 single base substitution C A downstream_gene_variant THCA-SA 15 42119603 42119603 single base substitution C T 3_prime_UTR_variant THCA-SA 15 42119603 42119603 single base substitution C T downstream_gene_variant THCA-SA 15 42119606 42119606 single base substitution C T 3_prime_UTR_variant THCA-SA 15 42119606 42119606 single base substitution C T downstream_gene_variant THCA-SA 15 42119711 42119711 single base substitution G A 3_prime_UTR_variant THCA-SA 15 42119711 42119711 single base substitution G A downstream_gene_variant THCA-SA 15 42119900 42119900 single base substitution T C 3_prime_UTR_variant THCA-SA 15 42119900 42119900 single base substitution T C downstream_gene_variant THCA-US 15 42114280 42114280 single base substitution C T 3_prime_UTR_variant THCA-US 15 42114280 42114280 single base substitution C T exon_variant THCA-US 15 42114280 42114280 single base substitution C T synonymous_variant C1001C 3003C>T THCA-US 15 42114280 42114280 single base substitution C T synonymous_variant C1007C 3021C>T THCA-US 15 42114280 42114280 single base substitution C T synonymous_variant C840C 2520C>T THCA-US 15 42114280 42114280 single base substitution C T synonymous_variant C884C 2652C>T THCA-US 15 42114280 42114280 single base substitution C T upstream_gene_variant THCA-US 15 42115281 42115281 single base substitution C T 3_prime_UTR_variant THCA-US 15 42115281 42115281 single base substitution C T downstream_gene_variant THCA-US 15 42115281 42115281 single base substitution C T exon_variant THCA-US 15 42115281 42115281 single base substitution C T intron_variant THCA-US 15 42115281 42115281 single base substitution C T synonymous_variant S1036S 3108C>T THCA-US 15 42115281 42115281 single base substitution C T synonymous_variant S1153S 3459C>T THCA-US 15 42115281 42115281 single base substitution C T synonymous_variant S1159S 3477C>T THCA-US 15 42115281 42115281 single base substitution C T synonymous_variant S992S 2976C>T UCEC-US 15 42104215 42104215 single base substitution C T 3_prime_UTR_variant UCEC-US 15 42104215 42104215 single base substitution C T downstream_gene_variant UCEC-US 15 42104215 42104215 single base substitution C T exon_variant UCEC-US 15 42104215 42104215 single base substitution C T synonymous_variant L130L 388C>T UCEC-US 15 42104215 42104215 single base substitution C T synonymous_variant L18L 52C>T UCEC-US 15 42104215 42104215 single base substitution C T upstream_gene_variant UCEC-US 15 42104263 42104263 single base substitution G A 3_prime_UTR_variant UCEC-US 15 42104263 42104263 single base substitution G A downstream_gene_variant UCEC-US 15 42104263 42104263 single base substitution G A exon_variant UCEC-US 15 42104263 42104263 single base substitution G A missense_variant A146T 436G>A UCEC-US 15 42104263 42104263 single base substitution G A missense_variant A34T 100G>A UCEC-US 15 42104263 42104263 single base substitution G A upstream_gene_variant UCEC-US 15 42104718 42104718 single base substitution A G 3_prime_UTR_variant UCEC-US 15 42104718 42104718 single base substitution A G downstream_gene_variant UCEC-US 15 42104718 42104718 single base substitution A G exon_variant UCEC-US 15 42104718 42104718 single base substitution A G missense_variant N168S 503A>G UCEC-US 15 42104718 42104718 single base substitution A G missense_variant N56S 167A>G UCEC-US 15 42104718 42104718 single base substitution A G upstream_gene_variant UCEC-US 15 42104788 42104788 single base substitution C G 3_prime_UTR_variant UCEC-US 15 42104788 42104788 single base substitution C G downstream_gene_variant UCEC-US 15 42104788 42104788 single base substitution C G exon_variant UCEC-US 15 42104788 42104788 single base substitution C G stop_gained Y191* 573C>G UCEC-US 15 42104788 42104788 single base substitution C G stop_gained Y79* 237C>G UCEC-US 15 42104788 42104788 single base substitution C G upstream_gene_variant UCEC-US 15 42105267 42105267 single base substitution C T 3_prime_UTR_variant UCEC-US 15 42105267 42105267 single base substitution C T downstream_gene_variant UCEC-US 15 42105267 42105267 single base substitution C T exon_variant UCEC-US 15 42105267 42105267 single base substitution C T stop_gained R151* 451C>T UCEC-US 15 42105267 42105267 single base substitution C T stop_gained R263* 787C>T UCEC-US 15 42105267 42105267 single base substitution C T upstream_gene_variant UCEC-US 15 42107465 42107465 single base substitution C T downstream_gene_variant UCEC-US 15 42107465 42107465 single base substitution C T exon_variant UCEC-US 15 42107465 42107465 single base substitution C T intron_variant UCEC-US 15 42107465 42107465 single base substitution C T synonymous_variant P276P 828C>T UCEC-US 15 42107465 42107465 single base substitution C T synonymous_variant P393P 1179C>T UCEC-US 15 42107465 42107465 single base substitution C T synonymous_variant P399P 1197C>T UCEC-US 15 42107465 42107465 single base substitution C T upstream_gene_variant UCEC-US 15 42107505 42107505 single base substitution T C 3_prime_UTR_variant UCEC-US 15 42107505 42107505 single base substitution T C downstream_gene_variant UCEC-US 15 42107505 42107505 single base substitution T C exon_variant UCEC-US 15 42107505 42107505 single base substitution T C intron_variant UCEC-US 15 42107505 42107505 single base substitution T C missense_variant S290P 868T>C UCEC-US 15 42107505 42107505 single base substitution T C missense_variant S407P 1219T>C UCEC-US 15 42107505 42107505 single base substitution T C missense_variant S413P 1237T>C UCEC-US 15 42107505 42107505 single base substitution T C upstream_gene_variant UCEC-US 15 42107555 42107555 single base substitution G A 3_prime_UTR_variant UCEC-US 15 42107555 42107555 single base substitution G A downstream_gene_variant UCEC-US 15 42107555 42107555 single base substitution G A exon_variant UCEC-US 15 42107555 42107555 single base substitution G A intron_variant UCEC-US 15 42107555 42107555 single base substitution G A synonymous_variant E306E 918G>A UCEC-US 15 42107555 42107555 single base substitution G A synonymous_variant E423E 1269G>A UCEC-US 15 42107555 42107555 single base substitution G A synonymous_variant E429E 1287G>A UCEC-US 15 42107555 42107555 single base substitution G A upstream_gene_variant UCEC-US 15 42107836 42107836 single base substitution C A 3_prime_UTR_variant UCEC-US 15 42107836 42107836 single base substitution C A downstream_gene_variant UCEC-US 15 42107836 42107836 single base substitution C A exon_variant UCEC-US 15 42107836 42107836 single base substitution C A synonymous_variant I283I 849C>A UCEC-US 15 42107836 42107836 single base substitution C A synonymous_variant I327I 981C>A UCEC-US 15 42107836 42107836 single base substitution C A synonymous_variant I444I 1332C>A UCEC-US 15 42107836 42107836 single base substitution C A synonymous_variant I450I 1350C>A UCEC-US 15 42107836 42107836 single base substitution C A upstream_gene_variant UCEC-US 15 42109643 42109643 single base substitution G A 3_prime_UTR_variant UCEC-US 15 42109643 42109643 single base substitution G A downstream_gene_variant UCEC-US 15 42109643 42109643 single base substitution G A exon_variant UCEC-US 15 42109643 42109643 single base substitution G A missense_variant R429H 1286G>A UCEC-US 15 42109643 42109643 single base substitution G A missense_variant R473H 1418G>A UCEC-US 15 42109643 42109643 single base substitution G A missense_variant R590H 1769G>A UCEC-US 15 42109643 42109643 single base substitution G A missense_variant R596H 1787G>A UCEC-US 15 42109643 42109643 single base substitution G A upstream_gene_variant UCEC-US 15 42109932 42109932 single base substitution C T downstream_gene_variant UCEC-US 15 42109932 42109932 single base substitution C T missense_variant R474W 1420C>T UCEC-US 15 42109932 42109932 single base substitution C T missense_variant R518W 1552C>T UCEC-US 15 42109932 42109932 single base substitution C T missense_variant R635W 1903C>T UCEC-US 15 42109932 42109932 single base substitution C T missense_variant R641W 1921C>T UCEC-US 15 42109932 42109932 single base substitution C T splice_region_variant UCEC-US 15 42109932 42109932 single base substitution C T upstream_gene_variant UCEC-US 15 42110463 42110463 single base substitution C A 3_prime_UTR_variant UCEC-US 15 42110463 42110463 single base substitution C A downstream_gene_variant UCEC-US 15 42110463 42110463 single base substitution C A exon_variant UCEC-US 15 42110463 42110463 single base substitution C A missense_variant F523L 1569C>A UCEC-US 15 42110463 42110463 single base substitution C A missense_variant F567L 1701C>A UCEC-US 15 42110463 42110463 single base substitution C A missense_variant F684L 2052C>A UCEC-US 15 42110463 42110463 single base substitution C A missense_variant F690L 2070C>A UCEC-US 15 42110463 42110463 single base substitution C A upstream_gene_variant UCEC-US 15 42110725 42110725 single base substitution A G 3_prime_UTR_variant UCEC-US 15 42110725 42110725 single base substitution A G downstream_gene_variant UCEC-US 15 42110725 42110725 single base substitution A G exon_variant UCEC-US 15 42110725 42110725 single base substitution A G missense_variant T540A 1618A>G UCEC-US 15 42110725 42110725 single base substitution A G missense_variant T584A 1750A>G UCEC-US 15 42110725 42110725 single base substitution A G missense_variant T701A 2101A>G UCEC-US 15 42110725 42110725 single base substitution A G missense_variant T707A 2119A>G UCEC-US 15 42110725 42110725 single base substitution A G upstream_gene_variant UCEC-US 15 42113808 42113808 single base substitution T G 3_prime_UTR_variant UCEC-US 15 42113808 42113808 single base substitution T G downstream_gene_variant UCEC-US 15 42113808 42113808 single base substitution T G exon_variant UCEC-US 15 42113808 42113808 single base substitution T G synonymous_variant A754A 2262T>G UCEC-US 15 42113808 42113808 single base substitution T G synonymous_variant A798A 2394T>G UCEC-US 15 42113808 42113808 single base substitution T G synonymous_variant A915A 2745T>G UCEC-US 15 42113808 42113808 single base substitution T G synonymous_variant A921A 2763T>G UCEC-US 15 42113808 42113808 single base substitution T G upstream_gene_variant UCEC-US 15 42114483 42114483 single base substitution C T 3_prime_UTR_variant UCEC-US 15 42114483 42114483 single base substitution C T exon_variant UCEC-US 15 42114483 42114483 single base substitution C T missense_variant A1031V 3092C>T UCEC-US 15 42114483 42114483 single base substitution C T missense_variant A1037V 3110C>T UCEC-US 15 42114483 42114483 single base substitution C T missense_variant A870V 2609C>T UCEC-US 15 42114483 42114483 single base substitution C T missense_variant A914V 2741C>T UCEC-US 15 42114483 42114483 single base substitution C T upstream_gene_variant UCEC-US 15 42115683 42115683 single base substitution G A 3_prime_UTR_variant UCEC-US 15 42115683 42115683 single base substitution G A downstream_gene_variant UCEC-US 15 42115683 42115683 single base substitution G A exon_variant UCEC-US 15 42115683 42115683 single base substitution G A intron_variant UCEC-US 15 42115683 42115683 single base substitution G A missense_variant A1052T 3154G>A UCEC-US 15 42115683 42115683 single base substitution G A missense_variant A1096T 3286G>A UCEC-US 15 42115683 42115683 single base substitution G A missense_variant A1213T 3637G>A UCEC-US 15 42115683 42115683 single base substitution G A missense_variant A1219T 3655G>A UCEC-US 15 42115987 42115987 single base substitution G A 3_prime_UTR_variant UCEC-US 15 42115987 42115987 single base substitution G A downstream_gene_variant UCEC-US 15 42115987 42115987 single base substitution G A exon_variant UCEC-US 15 42115987 42115987 single base substitution G A intron_variant UCEC-US 15 42115987 42115987 single base substitution G A missense_variant R1153Q 3458G>A UCEC-US 15 42115987 42115987 single base substitution G A missense_variant R1197Q 3590G>A UCEC-US 15 42115987 42115987 single base substitution G A missense_variant R1314Q 3941G>A UCEC-US 15 42115987 42115987 single base substitution G A missense_variant R1320Q 3959G>A

Mutation - COSMIC Sample Name Mutation ID Mutation CDS Mutation AA Mutation Description Mutation Genome Position Mutation Strand HCC1954 COSM50406 c.2324C>T p.P775L Substitution - Missense 15:41819278-41819278 + TCGA-AP-A059-01 COSM961559 c.3637G>A p.A1213T Substitution - Missense 15:41823485-41823485 + T1764 COSM4700630 c.535C>T p.R179W Substitution - Missense 15:41812552-41812552 + T3118 COSM4700634 c.1112A>C p.K371T Substitution - Missense 15:41814681-41814681 + TCGA-FW-A3R5-06 COSM3886954 c.3990C>T p.F1330F Substitution - coding silent 15:41823820-41823820 + PT35 COSM5913690 c.1196C>T p.P399L Substitution - Missense 15:41815266-41815266 + TCGA-EE-A29M-06 COSM3501137 c.2845C>T p.P949S Substitution - Missense 15:41821692-41821692 + TCGA-D3-A51G-06 COSM3501126 c.1238C>T p.S413F Substitution - Missense 15:41815308-41815308 + pfg062T COSM4753658 c.1022A>C p.N341T Substitution - Missense 15:41814573-41814573 + HCC171 COSM3706562 c.2736+7C>G p.? Unknown 15:41821075-41821075 + CHC2362T COSM4957070 c.1839G>A p.V613V Substitution - coding silent 15:41817652-41817652 + T578 COSM4700644 c.2802C>A p.V934V Substitution - coding silent 15:41821667-41821667 + TC71 COSM4578223 c.3710C>A p.A1237D Substitution - Missense 15:41823540-41823540 + TCGA-RP-A695-06 COSM4896978 c.1265C>T p.T422I Substitution - Missense 15:41815335-41815335 + TCGA-BS-A0UF-01 COSM961551 c.1332C>A p.I444I Substitution - coding silent 15:41815638-41815638 + TCGA-ER-A3PL-06 COSM3501132 c.2012C>T p.P671L Substitution - Missense 15:41818207-41818207 + TCGA-AP-A059-01 COSM961550 c.1269G>A p.E423E Substitution - coding silent 15:41815357-41815357 + TCGA-CD-5802-01 COSM4054602 c.3750C>A p.A1250A Substitution - coding silent 15:41823598-41823598 + TCGA-B4-5844-01 COSM1493379 c.2730C>A p.P910P Substitution - coding silent 15:41821595-41821595 + pfg181T COSM4747072 c.1194delC p.E400fs*2 Deletion - Frameshift 15:41815264-41815264 + PTC-7C COSM4148751 c.1719T>C p.V573V Substitution - coding silent 15:41817025-41817025 + TCGA-EJ-7797-01 COSM1470728 c.830C>A p.A277D Substitution - Missense 15:41813631-41813631 + ESCC_158 COSM5646649 c.323G>C p.G108A Substitution - Missense 15:41811231-41811231 + TCGA-BG-A0M6-01 COSM961556 c.2326G>T p.A776S Substitution - Missense 15:41819280-41819280 + PT46 COSM5929588 c.3325C>T p.P1109S Substitution - Missense 15:41822949-41822949 + TCGA-FS-A1ZA-06 COSM3501147 c.4370C>T p.S1457L Substitution - Missense 15:41825279-41825279 + TCGA-22-1012-01 COSM700627 c.1904+1G>T p.? Unknown 15:41817736-41817736 + TCGA-BR-4292-01 COSM4054586 c.756G>A p.T252T Substitution - coding silent 15:41813038-41813038 + TCGA-BR-8591-01 COSM4054592 c.1748C>T p.A583V Substitution - Missense 15:41817424-41817424 + TCGA-BH-A0W7-01 COSM5218023 c.559G>A p.E187K Substitution - Missense 15:41812576-41812576 + BON-1 COSM5368217 c.2224C>T p.R742C Substitution - Missense 15:41818890-41818890 + SM-4AX85 COSM5035076 c.937C>G p.L313V Substitution - Missense 15:41813720-41813720 + ccRCC-75 COSM1662695 c.2677A>G p.K893E Substitution - Missense 15:41821027-41821027 + T3417 COSM4700639 c.2086G>A p.V696M Substitution - Missense 15:41818281-41818281 + 2492703 COSM5599896 c.2767C>T p.H923Y Substitution - Missense 15:41821632-41821632 + ATL059 COSM5705863 c.4337G>A p.R1446Q Substitution - Missense 15:41825246-41825246 + MOLT-4 COSM1678386 c.1607C>T p.A536V Substitution - Missense 15:41816931-41816931 + TCGA-FU-A3HY-01 COSM4838536 c.92G>A p.R31Q Substitution - Missense 15:41775367-41775367 + HCC142T COSM1608358 c.3853C>G p.P1285A Substitution - Missense 15:41823701-41823701 + TCGA-EU-5904-01 COSM240603 c.1646G>A p.R549Q Substitution - Missense 15:41816970-41816970 + T2664 COSM4412677 c.3841C>T p.R1281* Substitution - Nonsense 15:41823671-41823671 + SM-4AX85 COSM5035081 c.1436G>A p.R479H Substitution - Missense 15:41815724-41815724 + TCGA-28-2509-01 COSM3747974 c.16T>G p.S6A Substitution - Missense 15:41775291-41775291 + Au2 COSM5599896 c.2767C>T p.H923Y Substitution - Missense 15:41821632-41821632 + TCGA-06-0174-01 COSM3401724 c.2307C>T p.N769N Substitution - coding silent 15:41818955-41818955 + 35M COSM5581619 c.1221C>T p.S407S Substitution - coding silent 15:41815309-41815309 + D10 COSM5007062 c.774C>T p.C258C Substitution - coding silent 15:41813056-41813056 + PT34 COSM5910859 c.207-5C>T p.? Unknown 15:41810878-41810878 + TCGA-Q1-A73O-01 COSM4836165 c.1390G>C p.E464Q Substitution - Missense 15:41815678-41815678 + TCGA-GF-A6C9-06 COSM4903778 c.663C>T p.G221G Substitution - coding silent 15:41812945-41812945 + TCGA-EE-A3J7-06 COSM3886957 c.3973C>T p.P1325S Substitution - Missense 15:41823821-41823821 + LS180 COSM2186341 c.865T>C p.C289R Substitution - Missense 15:41813666-41813666 + TCGA-E9-A1N4-01 COSM1478106 c.2293C>T p.H765Y Substitution - Missense 15:41819247-41819247 + DN11135 COSM5782302 c.2581G>A p.G861S Substitution - Missense 15:41820913-41820913 + TCGA-EK-A2RO-01 COSM4848696 c.4006G>T p.E1336* Substitution - Nonsense 15:41823854-41823854 + HX32T COSM3706567 c.4544G>A p.*1515* Substitution - coding silent 15:41825435-41825435 + HCT15 COSM4250991 c.2566C>T p.R856C Substitution - Missense 15:41820898-41820898 + TCGA-06-5856-01 COSM3401720 c.1197C>T p.P399P Substitution - coding silent 15:41815267-41815267 + LUAD-S00488 COSM395000 c.3941G>A p.R1314Q Substitution - Missense 15:41823789-41823789 + TCGA-FW-A3R5-06 COSM3886953 c.2695C>T p.L899F Substitution - Missense 15:41821045-41821045 + RK308_C01 COSM3744600 c.1938G>A p.K646K Substitution - coding silent 15:41818042-41818042 + TCGA-G2-A2EO-01 COSM1301119 c.172G>A p.D58N Substitution - Missense 15:41799880-41799880 + PCSI_0083_Pa_X COSM3377559 c.790A>C p.R264R Substitution - coding silent 15:41813072-41813072 + TCGA-AA-3663-01 COSM5101044 c.764G>T p.G255V Substitution - Missense 15:41813046-41813046 + YURAY COSM5383278 c.1728C>T p.V576V Substitution - coding silent 15:41817404-41817404 + Pat_76_B COSM5849140 c.884C>T p.T295I Substitution - Missense 15:41813685-41813685 + YUSPO COSM5383276 c.1451A>G p.N484S Substitution - Missense 15:41815757-41815757 + ESOSCC162T COSM1172259 c.935G>A p.R312Q Substitution - Missense 15:41813736-41813736 + MedB-1 COSM5621216 c.2141A>G p.D714G Substitution - Missense 15:41818549-41818549 + TCGA-CG-4306-01 COSM4054582 c.662G>A p.G221D Substitution - Missense 15:41812944-41812944 + DN11135 COSM5782303 c.2563G>A p.G855S Substitution - Missense 15:41820913-41820913 + TCGA-AA-A010-01 COSM282665 c.4116C>A p.L1372L Substitution - coding silent 15:41823964-41823964 + TCGA-BR-4184-01 COSM4054588 c.757T>A p.S253T Substitution - Missense 15:41813039-41813039 + TCGA-DI-A0WH-01 COSM961546 c.772T>A p.C258S Substitution - Missense 15:41813054-41813054 + TCGA-DJ-A4UW-01 COSM3370166 c.3003C>T p.C1001C Substitution - coding silent 15:41822082-41822082 + RK051_C01 COSM1629543 c.2426-2A>G p.? Unknown 15:41819593-41819593 + TCGA-FS-A1ZA-06 COSM3501146 c.4388C>T p.S1463L Substitution - Missense 15:41825279-41825279 + CHC892T COSM4798076 c.1000G>A p.A334T Substitution - Missense 15:41814569-41814569 + TCGA-EB-A5UN-06 COSM3501131 c.1875G>A p.T625T Substitution - coding silent 15:41817706-41817706 + 418 COSM4431827 c.3616+3G>T p.? Unknown 15:41823225-41823225 + T2664 COSM4412678 c.3823C>T p.R1275* Substitution - Nonsense 15:41823671-41823671 + TCGA-AA-3875-01 COSM272155 c.967G>A p.V323I Substitution - Missense 15:41813768-41813768 + TCGA-AA-3875-01 COSM272156 c.1198C>T p.Q400* Substitution - Nonsense 15:41815286-41815286 + T578 COSM4700631 c.936C>T p.F312F Substitution - coding silent 15:41813719-41813719 + PTC-7C COSM4148752 c.2492T>A p.M831K Substitution - Missense 15:41819643-41819643 + CSCC-11-T COSM4475880 c.2004C>T p.I668I Substitution - coding silent 15:41818217-41818217 + BD124T COSM5493263 c.1619G>A p.R540Q Substitution - Missense 15:41816943-41816943 + HCC066T COSM5821185 c.4295A>T p.Q1432L Substitution - Missense 15:41824547-41824547 + YUPAER COSM5383272 c.229_230CC>TT p.P77F Substitution - Missense 15:41810905-41810906 + TCGA-CD-8531-01 COSM4054598 c.2174G>A p.R725H Substitution - Missense 15:41818840-41818840 + TCGA-G2-A2EO-01 COSM1301118 c.158G>T p.R53I Substitution - Missense 15:41799866-41799866 + PT35 COSM5913692 c.3479T>G p.V1160G Substitution - Missense 15:41823103-41823103 + Pat_41_B COSM4250951 c.704C>T p.T235I Substitution - Missense 15:41812986-41812986 + MO_1249 COSM5566521 c.1844G>A p.R615Q Substitution - Missense 15:41817657-41817657 + 6115234 COSM5564009 c.2736G>A p.Q912Q Substitution - coding silent 15:41821068-41821068 + PTC-7C COSM4148757 c.3701G>C p.R1234P Substitution - Missense 15:41823549-41823549 + MedB-1 COSM5621217 c.2123A>G p.D708G Substitution - Missense 15:41818549-41818549 + CHC2362T COSM4957071 c.1821G>A p.V607V Substitution - coding silent 15:41817652-41817652 + TCGA-BP-5177-01 COSM470617 c.1540C>A p.H514N Substitution - Missense 15:41816605-41816605 + TCGA-DM-A1D6-01 COSM5167378 c.4280G>A p.R1427H Substitution - Missense 15:41824532-41824532 + T25 COSM5035076 c.937C>G p.L313V Substitution - Missense 15:41813720-41813720 + PTC_279 COSM5959584 c.3559C>T p.L1187F Substitution - Missense 15:41823183-41823183 + LUAD-RT-S01702 COSM298292 c.1209_1210insC p.S406fs*35 Insertion - Frameshift 15:41815297-41815298 + LIM2405 COSM4613393 c.3206_3207delCT p.L1070fs*59 Deletion - Frameshift 15:41822399-41822400 + TCGA-EE-A29E-06 COSM3501136 c.2452C>T p.P818S Substitution - Missense 15:41819603-41819603 + ESCC_102 COSM5638024 c.38A>C p.K13T Substitution - Missense 15:41775313-41775313 + MedB-1 COSM5621219 c.3602G>A p.R1201K Substitution - Missense 15:41823450-41823450 + LIM2551 COSM4643895 c.4479C>A p.A1493A Substitution - coding silent 15:41825370-41825370 + TCGA-EE-A29E-06 COSM84284 c.2434C>T p.P812S Substitution - Missense 15:41819603-41819603 + TCGA-FW-A3R5-06 COSM3886950 c.2511C>T p.S837S Substitution - coding silent 15:41820843-41820843 + BD124T COSM5493265 c.3354G>A p.S1118S Substitution - coding silent 15:41822978-41822978 + AOCS-120-3-6 COSM3981496 c.2734C>T p.R912W Substitution - Missense 15:41821599-41821599 + CSCC-29-T COSM4565581 c.2242_2243GG>AA p.G748N Substitution - Missense 15:41818908-41818909 + HCC171T COSM3706563 c.2718+7C>G p.? Unknown 15:41821075-41821075 + TCGA-D9-A6EC-06 COSM4402529 c.2252A>G p.Q751R Substitution - Missense 15:41818900-41818900 + PD8995a COSM5782303 c.2563G>A p.G855S Substitution - Missense 15:41820913-41820913 + SNU-C2B COSM4250964 c.1270C>T p.R424C Substitution - Missense 15:41815340-41815340 + TCGA-GF-A6C9-06 COSM4903777 c.663C>T p.G221G Substitution - coding silent 15:41812945-41812945 + TCGA-EE-A29M-06 COSM3501139 c.3068C>T p.P1023L Substitution - Missense 15:41822243-41822243 + pfg082T COSM4765194 c.726_727insA p.A245fs*18 Insertion - Frameshift 15:41813008-41813009 + TCGA-B2-3924-01 COSM470616 c.1463T>A p.L488Q Substitution - Missense 15:41815769-41815769 + PTC-7C COSM4148755 c.3108A>G p.E1036E Substitution - coding silent 15:41822301-41822301 + TCGA-AP-A059-01 COSM395000 c.3941G>A p.R1314Q Substitution - Missense 15:41823789-41823789 + LUAD_E00522 COSM352558 c.3902G>A p.R1301H Substitution - Missense 15:41823750-41823750 + TCGA-B5-A11G-01 COSM961548 c.1179C>T p.P393P Substitution - coding silent 15:41815267-41815267 + TCGA-DM-A1D6-01 COSM1372844 c.4262G>A p.R1421H Substitution - Missense 15:41824532-41824532 + HRA19 COSM4637731 c.2362G>A p.E788K Substitution - Missense 15:41819316-41819316 + CSCC-29-T COSM4565580 c.2260_2261GG>AA p.G754N Substitution - Missense 15:41818908-41818909 + TCGA-FW-A3R5-06 COSM3886955 c.3972C>T p.F1324F Substitution - coding silent 15:41823820-41823820 + HCC128 COSM1608357 c.3229+1G>C p.? Unknown 15:41822423-41822423 + TCGA-AG-4008-01 COSM259129 c.1167delG p.E390fs*6 Deletion - Frameshift 15:41814736-41814736 + BD124T COSM5493262 c.1637G>A p.R546Q Substitution - Missense 15:41816943-41816943 + TCGA-16-0861-01 COSM3401721 c.1658C>T p.A553V Substitution - Missense 15:41816964-41816964 + TCGA-06-0174-01 COSM42768 c.2289C>T p.N763N Substitution - coding silent 15:41818955-41818955 + 468 COSM4437432 c.2766C>G p.S922S Substitution - coding silent 15:41821613-41821613 + HCC68 COSM3706561 c.1791T>A p.T597T Substitution - coding silent 15:41817449-41817449 + LS174T COSM4250955 c.883T>C p.C295R Substitution - Missense 15:41813666-41813666 + WA16 COSM240603 c.1646G>A p.R549Q Substitution - Missense 15:41816970-41816970 + SNUH_G76_S1 COSM4148757 c.3701G>C p.R1234P Substitution - Missense 15:41823549-41823549 + TCGA-AX-A0J1-01 COSM961552 c.1769G>A p.R590H Substitution - Missense 15:41817445-41817445 + LIM2405 COSM4613392 c.3224_3225delCT p.L1076fs*59 Deletion - Frameshift 15:41822399-41822400 + TCGA-06-2563-01 COSM268136 c.2210G>A p.R737H Substitution - Missense 15:41818876-41818876 + TCGA-BS-A0UF-01 COSM961547 c.787C>T p.R263* Substitution - Nonsense 15:41813069-41813069 + cSCCP8 COSM140741 c.685C>A p.L229I Substitution - Missense 15:41812967-41812967 + TCGA-06-2563-01 COSM2152833 c.1002G>A p.A334A Substitution - coding silent 15:41814571-41814571 + Pat_24_A COSM5849145 c.3727C>T p.R1243W Substitution - Missense 15:41823557-41823557 + 43 COSM98006 c.2002A>T p.I668F Substitution - Missense 15:41818215-41818215 + 43 COSM98006 c.2002A>T p.I668F Substitution - Missense 15:41818215-41818215 + sysucc-880T COSM5462456 c.3328T>C p.S1110P Substitution - Missense 15:41822952-41822952 + TCGA-FD-A3SJ-01 COSM3794152 c.2512G>A p.V838M Substitution - Missense 15:41820844-41820844 + 587256 COSM1214550 c.1095G>T p.W365C Substitution - Missense 15:41814664-41814664 + DLD1 COSM1678387 c.2548C>T p.R850C Substitution - Missense 15:41820898-41820898 + HCT-15 COSM1678387 c.2548C>T p.R850C Substitution - Missense 15:41820898-41820898 + TCGA-GN-A262-06 COSM2186398 c.3704C>T p.P1235L Substitution - Missense 15:41823552-41823552 + CHC2362T COSM4957071 c.1821G>A p.V607V Substitution - coding silent 15:41817652-41817652 + PT49 COSM5936138 c.3412C>T p.P1138S Substitution - Missense 15:41823036-41823036 + TCGA-66-2789-01 COSM700631 c.1029C>T p.A343A Substitution - coding silent 15:41814598-41814598 + TCGA-06-2563 COSM268136 c.2210G>A p.R737H Substitution - Missense 15:41818876-41818876 + D10 COSM5007063 c.774C>T p.C258C Substitution - coding silent 15:41813056-41813056 + TCGA-BH-A0HA-01 COSM5216886 c.1983C>T p.D661D Substitution - coding silent 15:41818069-41818069 + TCGA-BS-A0UF-01 COSM961553 c.1903C>T p.R635W Substitution - Missense 15:41817734-41817734 + I2L-P18-Tumor-Organoid COSM5362868 c.3370C>G p.P1124A Substitution - Missense 15:41822994-41822994 + TCGA-FD-A3SJ-01 COSM3794153 c.2494G>A p.V832M Substitution - Missense 15:41820844-41820844 + TCGA-ES-A2HT-01 COSM4938571 c.620A>G p.D207G Substitution - Missense 15:41812637-41812637 + LUAD-RT-S01818 COSM383859 c.2128A>T p.K710* Substitution - Nonsense 15:41818554-41818554 + YUSPO COSM5383275 c.1469A>G p.N490S Substitution - Missense 15:41815757-41815757 + Pat_41_B COSM2270951 c.704C>T p.T235I Substitution - Missense 15:41812986-41812986 + PT49 COSM5936135 c.3431C>T p.P1144L Substitution - Missense 15:41823037-41823037 + TCGA-EB-A5UN-06 COSM3501130 c.1893G>A p.T631T Substitution - coding silent 15:41817706-41817706 + BB16T COSM50407 c.1247C>A p.T416N Substitution - Missense 15:41815335-41815335 + ACINAR28 COSM1734467 c.2349G>T p.K783N Substitution - Missense 15:41819303-41819303 + 480 COSM4439128 c.1605G>A p.S535S Substitution - coding silent 15:41816929-41816929 + HCC171 COSM3706563 c.2718+7C>G p.? Unknown 15:41821075-41821075 + LC_S6 COSM1190890 c.4287_4288delGC p.Y1431fs*>78 Deletion - Frameshift 15:41824557-41824558 + PT34 COSM5910858 c.207-5C>T p.? Unknown 15:41810878-41810878 + TCGA-FP-A4BE-01 COSM4054580 c.37A>G p.K13E Substitution - Missense 15:41775312-41775312 + TCGA-BR-8487-01 COSM4054593 c.1826G>A p.R609Q Substitution - Missense 15:41817639-41817639 + TCGA-EJ-7125-01 COSM3672042 c.1345G>T p.G449W Substitution - Missense 15:41815651-41815651 + AOCS-120-3-6 COSM3981495 c.2752C>T p.R918W Substitution - Missense 15:41821599-41821599 + 6115234 COSM5564010 c.2718G>A p.Q906Q Substitution - coding silent 15:41821068-41821068 + TCGA-GN-A266-06 COSM3501121 c.59C>T p.S20F Substitution - Missense 15:41775334-41775334 + TCGA-18-3409-01 COSM700628 c.1178C>T p.P393L Substitution - Missense 15:41815266-41815266 + 35M COSM5581618 c.1239C>T p.S413S Substitution - coding silent 15:41815309-41815309 + TCGA-FS-A1ZF-06 COSM3501134 c.2244C>T p.R748R Substitution - coding silent 15:41818892-41818892 + 06-P2007 COSM4578219 c.1899C>T p.I633I Substitution - coding silent 15:41817712-41817712 + TCGA-AD-6889-01 COSM1372843 c.3657C>T p.I1219I Substitution - coding silent 15:41823505-41823505 + PCSI_0083_Pa_X COSM3377558 c.790A>C p.R264R Substitution - coding silent 15:41813072-41813072 + TCGA-E9-A1N4-01 COSM5229628 c.2311C>T p.H771Y Substitution - Missense 15:41819247-41819247 + YURAY COSM2186356 c.1729C>T p.R577C Substitution - Missense 15:41817405-41817405 + sysucc-1370T COSM5470345 c.2173C>T p.R725C Substitution - Missense 15:41818839-41818839 + TCGA-G4-6293-01 COSM5173989 c.486G>A p.V162V Substitution - coding silent 15:41812115-41812115 + sysucc-1370T COSM5470344 c.2191C>T p.R731C Substitution - Missense 15:41818839-41818839 + ESCC_158 COSM5646650 c.323G>C p.G108A Substitution - Missense 15:41811231-41811231 + Pat_14_B COSM5849138 c.569G>A p.S190N Substitution - Missense 15:41812586-41812586 + TCGA-D3-A51E-06 COSM3501143 c.4076C>T p.P1359L Substitution - Missense 15:41823924-41823924 + TCGA-BR-7703-01 COSM4054599 c.2470C>T p.R824* Substitution - Nonsense 15:41819621-41819621 + T3505 COSM4700626 c.325G>T p.E109* Substitution - Nonsense 15:41811233-41811233 + I2L-P18-Tumor-Organoid COSM5362867 c.3388C>G p.P1130A Substitution - Missense 15:41822994-41822994 + TCGA-DK-A1A3-01 COSM416940 c.1396G>A p.D466N Substitution - Missense 15:41815702-41815702 + CHC2362T COSM4957070 c.1839G>A p.V613V Substitution - coding silent 15:41817652-41817652 + SC_9022 COSM5563746 c.1354C>T p.Q452* Substitution - Nonsense 15:41815660-41815660 + PCSI_0090_Pa_X COSM3377560 c.3084C>T p.G1028G Substitution - coding silent 15:41822259-41822259 + TCGA-AA-3811-01 COSM293758 c.3159delC p.Q1055fs*9 Deletion - Frameshift 15:41822352-41822352 + LS174T COSM2186341 c.865T>C p.C289R Substitution - Missense 15:41813666-41813666 + TCGA-BR-7703-01 COSM4054590 c.1022C>T p.T341I Substitution - Missense 15:41814591-41814591 + SNU-175 COSM4250977 c.1921C>T p.R641W Substitution - Missense 15:41817734-41817734 + Pat_59_B COSM5849148 c.4192G>A p.A1398T Substitution - Missense 15:41824040-41824040 + T3351 COSM4700635 c.1158G>T p.L386L Substitution - coding silent 15:41814709-41814709 + TCGA-EE-A3J7-06 COSM3886956 c.3991C>T p.P1331S Substitution - Missense 15:41823821-41823821 + PT35 COSM700628 c.1178C>T p.P393L Substitution - Missense 15:41815266-41815266 + J30_T COSM700630 c.1177C>T p.P393S Substitution - Missense 15:41815265-41815265 + ESCC_102 COSM5638025 c.38A>C p.K13T Substitution - Missense 15:41775313-41775313 + 480 COSM4439127 c.1623G>A p.S541S Substitution - coding silent 15:41816929-41816929 + TCGA-D3-A51E-06 COSM3501142 c.4094C>T p.P1365L Substitution - Missense 15:41823924-41823924 + YURAY COSM4250972 c.1747C>T p.R583C Substitution - Missense 15:41817405-41817405 + T578 COSM4700632 c.918C>T p.F306F Substitution - coding silent 15:41813719-41813719 + TCGA-FW-A3R5-06 COSM3886952 c.2713C>T p.L905F Substitution - Missense 15:41821045-41821045 + TCGA-BQ-5876-01 COSM272155 c.967G>A p.V323I Substitution - Missense 15:41813768-41813768 + 418 COSM4431828 c.3598+3G>T p.? Unknown 15:41823225-41823225 + CSCC-49-T COSM4462071 c.1231C>T p.P411S Substitution - Missense 15:41815301-41815301 + T1764 COSM4700629 c.535C>T p.R179W Substitution - Missense 15:41812552-41812552 + pfg082T COSM4765193 c.726_727insA p.A245fs*18 Insertion - Frameshift 15:41813008-41813009 + RK189_C01 COSM1629544 c.4089T>C p.C1363C Substitution - coding silent 15:41823937-41823937 + PT49 COSM5936137 c.3430C>T p.P1144S Substitution - Missense 15:41823036-41823036 + TCGA-D9-A6EC-06 COSM961553 c.1903C>T p.R635W Substitution - Missense 15:41817734-41817734 + TCGA-FS-A1ZF-06 COSM3501135 c.2226C>T p.R742R Substitution - coding silent 15:41818892-41818892 + TCGA-A5-A0GB-01 COSM961543 c.388C>T p.L130L Substitution - coding silent 15:41812017-41812017 + 2492703 COSM5599895 c.2785C>T p.H929Y Substitution - Missense 15:41821632-41821632 + TCGA-B5-A11E-01 COSM961549 c.1219T>C p.S407P Substitution - Missense 15:41815307-41815307 + CSCC-16-T COSM4517815 c.430_431CC>TT p.P144F Substitution - Missense 15:41812059-41812060 + LS180 COSM4250955 c.883T>C p.C295R Substitution - Missense 15:41813666-41813666 + TC71 COSM4578224 c.3692C>A p.A1231D Substitution - Missense 15:41823540-41823540 + TCGA-AC-A23H-01 COSM3816038 c.3519C>G p.L1173L Substitution - coding silent 15:41823125-41823125 + TCGA-EB-A551-01 COSM3501144 c.4102C>T p.P1368S Substitution - Missense 15:41823932-41823932 + TCGA-28-2509-01 COSM3747975 c.16T>G p.S6A Substitution - Missense 15:41775291-41775291 + PT49 COSM5936136 c.3413C>T p.P1138L Substitution - Missense 15:41823037-41823037 + Pat_28_B COSM5849142 c.1925G>A p.G642E Substitution - Missense 15:41818029-41818029 + TCGA-DJ-A1QH-01 COSM3370168 c.3459C>T p.S1153S Substitution - coding silent 15:41823083-41823083 + PT44 COSM5926915 c.1477C>T p.R493C Substitution - Missense 15:41815783-41815783 + TCGA-FP-A4BE-01 COSM4054579 c.37A>G p.K13E Substitution - Missense 15:41775312-41775312 + I2L-P7-Tumor-Organoid COSM5363106 c.2630A>G p.Q877R Substitution - Missense 15:41820980-41820980 + 43T COSM109434 c.4072G>A p.G1358R Substitution - Missense 15:41823920-41823920 + T3446 COSM4700627 c.394G>T p.E132* Substitution - Nonsense 15:41812023-41812023 + CHC892T COSM4798075 c.1018G>A p.A340T Substitution - Missense 15:41814569-41814569 + TCGA-D3-A51G-06 COSM3501127 c.1220C>T p.S407F Substitution - Missense 15:41815308-41815308 + TCGA-BR-4370-01 COSM4054604 c.3964C>T p.P1322S Substitution - Missense 15:41823812-41823812 + SM-4AX84 COSM4412677 c.3841C>T p.R1281* Substitution - Nonsense 15:41823671-41823671 + TCGA-ES-A2HT-01 COSM4938572 c.620A>G p.D207G Substitution - Missense 15:41812637-41812637 + ATL059 COSM5705862 c.4355G>A p.R1452Q Substitution - Missense 15:41825246-41825246 + LUAD-CHTN-MAD06-00668 COSM391316 c.3411_3412insC p.G1140fs*31 Insertion - Frameshift 15:41823035-41823036 + Pat_51_A COSM5849144 c.1933A>C p.K645Q Substitution - Missense 15:41818037-41818037 + PT44 COSM5926914 c.1495C>T p.R499C Substitution - Missense 15:41815783-41815783 + CSCC-19-T COSM4566656 c.4355_4356GG>AA p.R1452Q Substitution - Missense 15:41825246-41825247 + TCGA-D7-A4Z0-01 COSM4054605 c.4153T>C p.L1385L Substitution - coding silent 15:41823983-41823983 + T2269 COSM4700642 c.2705C>A p.S902* Substitution - Nonsense 15:41821055-41821055 + sysucc-880T COSM5462455 c.3346T>C p.S1116P Substitution - Missense 15:41822952-41822952 + SNU-175 COSM961553 c.1903C>T p.R635W Substitution - Missense 15:41817734-41817734 + 2492701 COSM5599896 c.2767C>T p.H923Y Substitution - Missense 15:41821632-41821632 + PT19_2 COSM5900305 c.4186C>T p.P1396S Substitution - Missense 15:41824016-41824016 + TCGA-G4-6320-01 COSM2186409 c.4508G>A p.R1503H Substitution - Missense 15:41825417-41825417 + Pat_59_B COSM5849147 c.4210G>A p.A1404T Substitution - Missense 15:41824040-41824040 + TCGA-FU-A3HY-01 COSM4838535 c.92G>A p.R31Q Substitution - Missense 15:41775367-41775367 + 2492701 COSM5599895 c.2785C>T p.H929Y Substitution - Missense 15:41821632-41821632 + TCGA-EE-A2MP-06 COSM3501122 c.629C>T p.T210I Substitution - Missense 15:41812646-41812646 + LC_S12 COSM1190889 c.225delC p.F75fs*84 Deletion - Frameshift 15:41810901-41810901 + BD156T COSM5494602 c.1001G>A p.R334H Substitution - Missense 15:41814552-41814552 + TCGA-AZ-4315-01 COSM3690392 c.2053C>A p.L685I Substitution - Missense 15:41818248-41818248 + HCC128 COSM3706564 c.3247+1G>C p.? Unknown 15:41822423-41822423 + TCGA-DS-A1OC-01 COSM1293531 c.179G>A p.R60Q Substitution - Missense 15:41799887-41799887 + T1764 COSM4700637 c.1765G>A p.A589T Substitution - Missense 15:41817423-41817423 + CSCC-27-T COSM3886957 c.3973C>T p.P1325S Substitution - Missense 15:41823821-41823821 + TCGA-GN-A262-06 COSM3501141 c.3722C>T p.P1241L Substitution - Missense 15:41823552-41823552 + 587332 COSM1214548 c.2518G>A p.A840T Substitution - Missense 15:41820868-41820868 + KPOPBR-34-T COSM5963296 c.3567C>A p.P1189P Substitution - coding silent 15:41823173-41823173 + TCGA-06-2563 COSM2152833 c.1002G>A p.A334A Substitution - coding silent 15:41814571-41814571 + CSCC-27-T COSM3886956 c.3991C>T p.P1331S Substitution - Missense 15:41823821-41823821 + TCGA-D1-A16F-01 COSM961555 c.2101A>G p.T701A Substitution - Missense 15:41818527-41818527 + TCGA-D3-A5GU-06 COSM3501124 c.722G>A p.R241K Substitution - Missense 15:41813004-41813004 + SM-4AX85 COSM5035077 c.919C>G p.L307V Substitution - Missense 15:41813720-41813720 + PT35 COSM5913691 c.3497T>G p.V1166G Substitution - Missense 15:41823103-41823103 + MB108C COSM88045 c.536G>A p.R179Q Substitution - Missense 15:41812553-41812553 + TCGA-ER-A19F-06 COSM3501129 c.1428C>T p.I476I Substitution - coding silent 15:41815734-41815734 + CSCC-11-T COSM4475879 c.2022C>T p.I674I Substitution - coding silent 15:41818217-41818217 + 1731645 COSM327853 c.232C>G p.R78G Substitution - Missense 15:41810908-41810908 + OV207 COSM252598 c.1768C>T p.R590C Substitution - Missense 15:41817444-41817444 + HCC76 COSM1608359 c.4422C>A p.G1474G Substitution - coding silent 15:41825331-41825331 + TCGA-CD-5802-01 COSM4054601 c.3768C>A p.A1256A Substitution - coding silent 15:41823598-41823598 + YURAY COSM5383277 c.1746C>T p.V582V Substitution - coding silent 15:41817404-41817404 + 93VU147T COSM4591125 c.2777G>A p.R926Q Substitution - Missense 15:41821642-41821642 + TCGA-G4-6302-01 COSM2186382 c.2868C>T p.N956N Substitution - coding silent 15:41821733-41821733 + TCGA-D1-A17U-01 COSM961545 c.573C>G p.Y191* Substitution - Nonsense 15:41812590-41812590 + GC_370T-GC_370N COSM4773198 c.1353C>A p.T451T Substitution - coding silent 15:41815659-41815659 + ME044T COSM229268 c.2285C>T p.P762L Substitution - Missense 15:41818951-41818951 + TCGA-D3-A5GU-06 COSM3501125 c.722G>A p.R241K Substitution - Missense 15:41813004-41813004 + TCGA-BR-8487-01 COSM4054594 c.1808G>A p.R603Q Substitution - Missense 15:41817639-41817639 + pfg181T COSM4747073 c.1176delC p.E394fs*2 Deletion - Frameshift 15:41815264-41815264 + TCGA-G4-6320-01 COSM3690394 c.4526G>A p.R1509H Substitution - Missense 15:41825417-41825417 + ESCC_BICR_054T COSM5444200 c.2026G>A p.D676N Substitution - Missense 15:41818239-41818239 + TCGA-BR-7703-01 COSM4054589 c.1040C>T p.T347I Substitution - Missense 15:41814591-41814591 + HCC142 COSM1608358 c.3853C>G p.P1285A Substitution - Missense 15:41823701-41823701 + HCC066T COSM5821186 c.4277A>T p.Q1426L Substitution - Missense 15:41824547-41824547 + Detroit_562 COSM2186353 c.1461T>C p.H487H Substitution - coding silent 15:41815767-41815767 + TCGA-AA-A00N-01 COSM275992 c.2035C>A p.L679I Substitution - Missense 15:41818248-41818248 + TCGA-BR-8591-01 COSM4054591 c.1766C>T p.A589V Substitution - Missense 15:41817424-41817424 + CSCC-29-T COSM4492151 c.3922C>T p.P1308S Substitution - Missense 15:41823752-41823752 + TCGA-EE-A3JA-06 COSM3501127 c.1220C>T p.S407F Substitution - Missense 15:41815308-41815308 + TCGA-A3-3316-01 COSM1470728 c.830C>A p.A277D Substitution - Missense 15:41813631-41813631 + TCGA-BR-6852-01 COSM4054595 c.1977T>C p.G659G Substitution - coding silent 15:41818063-41818063 + LUAD-GU4I3 COSM341584 c.4144C>T p.P1382S Substitution - Missense 15:41823992-41823992 + TCGA-D7-A4Z0-01 COSM4054606 c.4135T>C p.L1379L Substitution - coding silent 15:41823983-41823983 + 2178 COSM5017192 c.4418G>T p.G1473V Substitution - Missense 15:41825309-41825309 + TCGA-ER-A3PL-06 COSM3501133 c.1994C>T p.P665L Substitution - Missense 15:41818207-41818207 + TCGA-AR-A0TU-01 COSM5210870 c.2667G>C p.S889S Substitution - coding silent 15:41820999-41820999 + C0098T COSM4150933 c.2709C>T p.L903L Substitution - coding silent 15:41821059-41821059 + HCT15 COSM1678387 c.2548C>T p.R850C Substitution - Missense 15:41820898-41820898 + 2492700 COSM5599896 c.2767C>T p.H923Y Substitution - Missense 15:41821632-41821632 + TCGA-CD-8531-01 COSM4054597 c.2192G>A p.R731H Substitution - Missense 15:41818840-41818840 + TCGA-AA-3684-01 COSM268136 c.2210G>A p.R737H Substitution - Missense 15:41818876-41818876 + HCC68T COSM1608356 c.1773T>A p.T591T Substitution - coding silent 15:41817449-41817449 + TCGA-DJ-A1QH-01 COSM3370167 c.3477C>T p.S1159S Substitution - coding silent 15:41823083-41823083 + SNU-175 COSM2186404 c.3982C>T p.L1328L Substitution - coding silent 15:41823830-41823830 + SNUH_G76_S1 COSM4148756 c.3719G>C p.R1240P Substitution - Missense 15:41823549-41823549 + TCGA-AA-3850-01 COSM295550 c.222G>A p.L74L Substitution - coding silent 15:41810898-41810898 + PTC-7C COSM1129211 c.1701T>C p.V567V Substitution - coding silent 15:41817025-41817025 + LUAD-F00057 COSM339326 c.3172G>A p.D1058N Substitution - Missense 15:41822365-41822365 + TCGA-D9-A6EC-06 COSM4250977 c.1921C>T p.R641W Substitution - Missense 15:41817734-41817734 + 449 COSM4435403 c.207-3C>T p.? Unknown 15:41810880-41810880 + LIM2551 COSM4643896 c.4461C>A p.A1487A Substitution - coding silent 15:41825370-41825370 + BD156T COSM5494603 c.983G>A p.R328H Substitution - Missense 15:41814552-41814552 + SM-4AX84 COSM4412678 c.3823C>T p.R1275* Substitution - Nonsense 15:41823671-41823671 + TCGA-CG-4306-01 COSM4054581 c.662G>A p.G221D Substitution - Missense 15:41812944-41812944 + TCGA-ER-A42K-06 COSM4894807 c.900C>G p.N300K Substitution - Missense 15:41813701-41813701 + TCGA-AD-6889-01 COSM5129451 c.3675C>T p.I1225I Substitution - coding silent 15:41823505-41823505 + I2L-P7-Tumor-Organoid COSM5363105 c.2648A>G p.Q883R Substitution - Missense 15:41820980-41820980 + T3446 COSM4700628 c.394G>T p.E132* Substitution - Nonsense 15:41812023-41812023 + YUPAER COSM5383279 c.2276C>T p.P759L Substitution - Missense 15:41818924-41818924 + 2492702 COSM5599895 c.2785C>T p.H929Y Substitution - Missense 15:41821632-41821632 + TCGA-AA-A00E-01 COSM298292 c.1209_1210insC p.S406fs*35 Insertion - Frameshift 15:41815297-41815298 + TCGA-DD-A113-01 COSM4925375 c.3406G>A p.A1136T Substitution - Missense 15:41823030-41823030 + TCGA-EE-A29M-06 COSM3501140 c.3050C>T p.P1017L Substitution - Missense 15:41822243-41822243 + TCGA-BR-4292-01 COSM4054585 c.756G>A p.T252T Substitution - coding silent 15:41813038-41813038 + 06-P036 COSM4578221 c.3411G>A p.P1137P Substitution - coding silent 15:41823017-41823017 + T3505 COSM4700625 c.325G>T p.E109* Substitution - Nonsense 15:41811233-41811233 + TCGA-BH-A0HA-01 COSM433842 c.1965C>T p.D655D Substitution - coding silent 15:41818069-41818069 + 43 COSM3722474 c.2020A>T p.I674F Substitution - Missense 15:41818215-41818215 + TCGA-18-3409-01 COSM700630 c.1177C>T p.P393S Substitution - Missense 15:41815265-41815265 + TCGA-BH-A0W7-01 COSM433841 c.559G>A p.E187K Substitution - Missense 15:41812576-41812576 + CHC892T COSM4798076 c.1000G>A p.A334T Substitution - Missense 15:41814569-41814569 + CHC892T COSM4798075 c.1018G>A p.A340T Substitution - Missense 15:41814569-41814569 + HCC142 COSM3706565 c.3871C>G p.P1291A Substitution - Missense 15:41823701-41823701 + PCSI_0090_Pa_X COSM3377561 c.3066C>T p.G1022G Substitution - coding silent 15:41822259-41822259 + TCGA-GN-A266-06 COSM3501120 c.59C>T p.S20F Substitution - Missense 15:41775334-41775334 + T25 COSM5035077 c.919C>G p.L307V Substitution - Missense 15:41813720-41813720 + TCGA-EJ-7123-01 COSM3672043 c.2017G>T p.G673W Substitution - Missense 15:41818212-41818212 + NPC15F COSM4995568 c.1103G>T p.R368M Substitution - Missense 15:41814672-41814672 + 90624 COSM330319 c.4516C>T p.R1506C Substitution - Missense 15:41825425-41825425 + TCGA-AA-3663-01 COSM1372841 c.764G>T p.G255V Substitution - Missense 15:41813046-41813046 + TCGA-06-2563-01 COSM3401723 c.2228G>A p.R743H Substitution - Missense 15:41818876-41818876 + Pat_76_A COSM5849139 c.902C>T p.T301I Substitution - Missense 15:41813685-41813685 + TCGA-E2-A153-01 COSM433844 c.3882C>T p.I1294I Substitution - coding silent 15:41823730-41823730 + HCC68 COSM1608356 c.1773T>A p.T591T Substitution - coding silent 15:41817449-41817449 + TCGA-EK-A2RO-01 COSM4848695 c.4024G>T p.E1342* Substitution - Nonsense 15:41823854-41823854 + Detroit_562 COSM4250968 c.1479T>C p.H493H Substitution - coding silent 15:41815767-41815767 + TCGA-BH-A18G-01 COSM3816037 c.3068T>C p.I1023T Substitution - Missense 15:41822261-41822261 + GC_370T-GC_370N COSM4773197 c.1371C>A p.T457T Substitution - coding silent 15:41815659-41815659 + C0098T COSM4150932 c.2727C>T p.L909L Substitution - coding silent 15:41821059-41821059 + TCGA-06-5856-01 COSM961548 c.1179C>T p.P393P Substitution - coding silent 15:41815267-41815267 + YUAKER COSM1708039 c.2047G>T p.D683Y Substitution - Missense 15:41818260-41818260 + SC_9022 COSM5563745 c.1372C>T p.Q458* Substitution - Nonsense 15:41815660-41815660 + TCGA-AA-A029-01 COSM300611 c.2703T>G p.T901T Substitution - coding silent 15:41821053-41821053 + TCGA-BR-6852-01 COSM4054596 c.1959T>C p.G653G Substitution - coding silent 15:41818063-41818063 + PTC-7C COSM4148756 c.3719G>C p.R1240P Substitution - Missense 15:41823549-41823549 + CSCC-29-T COSM4492152 c.3904C>T p.P1302S Substitution - Missense 15:41823752-41823752 + Pat_51_A COSM5849143 c.1951A>C p.K651Q Substitution - Missense 15:41818037-41818037 + DLD1 COSM4250991 c.2566C>T p.R856C Substitution - Missense 15:41820898-41820898 + TCGA-BQ-5876-01 COSM3987944 c.985G>A p.V329I Substitution - Missense 15:41813768-41813768 + HCC76 COSM3706566 c.4440C>A p.G1480G Substitution - coding silent 15:41825331-41825331 + sysucc-679T COSM5480602 c.1271G>A p.R424H Substitution - Missense 15:41815341-41815341 + HCC171T COSM3706562 c.2736+7C>G p.? Unknown 15:41821075-41821075 + NPC15F COSM4995567 c.1121G>T p.R374M Substitution - Missense 15:41814672-41814672 + Pat_76_A COSM5849140 c.884C>T p.T295I Substitution - Missense 15:41813685-41813685 + 468 COSM4437433 c.2748C>G p.S916S Substitution - coding silent 15:41821613-41821613 + TCGA-AZ-4315-01 COSM275992 c.2035C>A p.L679I Substitution - Missense 15:41818248-41818248 + TCGA-AP-A051-01 COSM433840 c.436G>A p.A146T Substitution - Missense 15:41812065-41812065 + Au2 COSM5599895 c.2785C>T p.H929Y Substitution - Missense 15:41821632-41821632 + SNU-175 COSM4251020 c.4000C>T p.L1334L Substitution - coding silent 15:41823830-41823830 + pfg062T COSM4753659 c.1004A>C p.N335T Substitution - Missense 15:41814573-41814573 + TCGA-29-2432-01 COSM1323212 c.1182G>A p.E394E Substitution - coding silent 15:41815270-41815270 + TCGA-EJ-7123-01 COSM3672044 c.1999G>T p.G667W Substitution - Missense 15:41818212-41818212 + 06-P036 COSM4578222 c.3393G>A p.P1131P Substitution - coding silent 15:41823017-41823017 + 449 COSM4435404 c.207-3C>T p.? Unknown 15:41810880-41810880 + HCC128T COSM1608357 c.3229+1G>C p.? Unknown 15:41822423-41822423 + TCGA-G4-6293-01 COSM1372840 c.486G>A p.V162V Substitution - coding silent 15:41812115-41812115 + sysucc-679T COSM5480603 c.1253G>A p.R418H Substitution - Missense 15:41815341-41815341 + ACINAR11 COSM1734468 c.2439C>G p.S813R Substitution - Missense 15:41819608-41819608 + Pat_14_B COSM5849137 c.569G>A p.S190N Substitution - Missense 15:41812586-41812586 + STC232 COSM5054281 c.3710G>A p.R1237Q Substitution - Missense 15:41823558-41823558 + HCT8 COSM1678387 c.2548C>T p.R850C Substitution - Missense 15:41820898-41820898 + ESCC_141 COSM4578221 c.3411G>A p.P1137P Substitution - coding silent 15:41823017-41823017 + YUNEKI COSM5383274 c.644_645CC>TT p.A215V Substitution - Missense 15:41812926-41812927 + TCGA-AC-A23H-01 COSM2186403 c.3952G>A p.E1318K Substitution - Missense 15:41823800-41823800 + TCGA-DD-A113-01 COSM4925374 c.3424G>A p.A1142T Substitution - Missense 15:41823030-41823030 + TCGA-ER-A19F-06 COSM3501128 c.1446C>T p.I482I Substitution - coding silent 15:41815734-41815734 + 2178 COSM5017193 c.4400G>T p.G1467V Substitution - Missense 15:41825309-41825309 + HCT8 COSM4250991 c.2566C>T p.R856C Substitution - Missense 15:41820898-41820898 + 587342 COSM1214549 c.2242G>A p.G748S Substitution - Missense 15:41818908-41818908 + RK169_C01 COSM3700952 c.1384G>T p.D462Y Substitution - Missense 15:41815672-41815672 + TCGA-AR-A0TU-01 COSM433843 c.2649G>C p.S883S Substitution - coding silent 15:41820999-41820999 + TCGA-BS-A0UF-01 COSM961554 c.2052C>A p.F684L Substitution - Missense 15:41818265-41818265 + YUNEKI COSM5383273 c.644_645CC>TT p.A215V Substitution - Missense 15:41812926-41812927 + TCGA-06-2563-01 COSM3401719 c.1020G>A p.A340A Substitution - coding silent 15:41814571-41814571 + TCGA-AC-A23H-01 COSM3816040 c.3970G>A p.E1324K Substitution - Missense 15:41823800-41823800 + HX32T COSM3706568 c.4526G>A p.*1509* Substitution - coding silent 15:41825435-41825435 + 169 COSM2186352 c.1314C>T p.S438S Substitution - coding silent 15:41815402-41815402 + TCGA-BS-A0UL-01 COSM961558 c.3092C>T p.A1031V Substitution - Missense 15:41822285-41822285 + TCGA-AP-A051-01 COSM961557 c.2745T>G p.A915A Substitution - coding silent 15:41821610-41821610 + TCGA-AC-A23H-01 COSM3816039 c.3501C>G p.L1167L Substitution - coding silent 15:41823125-41823125 + ESCC_141 COSM4578222 c.3393G>A p.P1131P Substitution - coding silent 15:41823017-41823017 + HN_62426 COSM124327 c.4153G>A p.E1385K Substitution - Missense 15:41824001-41824001 + T47 COSM1177588 c.2954A>G p.E985G Substitution - Missense 15:41822033-41822033 + TCGA-D9-A6EC-06 COSM4402530 c.2234A>G p.Q745R Substitution - Missense 15:41818900-41818900 + TCGA-ER-A42K-06 COSM4894806 c.918C>G p.N306K Substitution - Missense 15:41813701-41813701 + MO_1249 COSM5566522 c.1826G>A p.R609Q Substitution - Missense 15:41817657-41817657 + CSCC-19-T COSM4566657 c.4337_4338GG>AA p.R1446Q Substitution - Missense 15:41825246-41825247 + HRA19 COSM4637730 c.2380G>A p.E794K Substitution - Missense 15:41819316-41819316 + TCGA-FW-A3R5-06 COSM3886951 c.2493C>T p.S831S Substitution - coding silent 15:41820843-41820843 + TCGA-Q1-A73O-01 COSM4836166 c.1372G>C p.E458Q Substitution - Missense 15:41815678-41815678 + 10-104 COSM3736608 c.530C>T p.S177F Substitution - Missense 15:41812547-41812547 + TCGA-EE-A29M-06 COSM3501138 c.2827C>T p.P943S Substitution - Missense 15:41821692-41821692 + J30_T COSM3956618 c.1195C>T p.P399S Substitution - Missense 15:41815265-41815265 + TCGA-EE-A2MP-06 COSM3501123 c.629C>T p.T210I Substitution - Missense 15:41812646-41812646 + HCC011T COSM5819990 c.1068T>G p.N356K Substitution - Missense 15:41814619-41814619 + HCC1954 COSM50406 c.2324C>T p.P775L Substitution - Missense 15:41819278-41819278 + TCGA-DJ-A4UW-01 COSM3370165 c.3021C>T p.C1007C Substitution - coding silent 15:41822082-41822082 + T3351 COSM4700636 c.1140G>T p.L380L Substitution - coding silent 15:41814709-41814709 + PD3857a COSM162383 c.2735G>T p.R912L Substitution - Missense 15:41821600-41821600 + TCGA-BR-8059-01 COSM4054584 c.673C>T p.L225L Substitution - coding silent 15:41812955-41812955 + CSCC-49-T COSM4462072 c.1213C>T p.P405S Substitution - Missense 15:41815301-41815301 + SNU-C2B COSM2186349 c.1252C>T p.R418C Substitution - Missense 15:41815340-41815340 + T2269 COSM4700641 c.2723C>A p.S908* Substitution - Nonsense 15:41821055-41821055 + YUPAER COSM5383280 c.2258C>T p.P753L Substitution - Missense 15:41818924-41818924 + TCGA-B5-A11E-01 COSM961544 c.503A>G p.N168S Substitution - Missense 15:41812520-41812520 + CSCC-16-T COSM4517816 c.430_431CC>TT p.P144F Substitution - Missense 15:41812059-41812060 + PD4106a COSM162384 c.1337A>G p.Y446C Substitution - Missense 15:41815643-41815643 + TCGA-AR-A0U3-01 COSM433840 c.436G>A p.A146T Substitution - Missense 15:41812065-41812065 + Pa10X COSM84284 c.2434C>T p.P812S Substitution - Missense 15:41819603-41819603 + SM-4AX85 COSM5035082 c.1418G>A p.R473H Substitution - Missense 15:41815724-41815724 + PTC_279 COSM5959583 c.3577C>T p.L1193F Substitution - Missense 15:41823183-41823183 + PTC-7C COSM4148754 c.3126A>G p.E1042E Substitution - coding silent 15:41822301-41822301 + Pat_28_B COSM5849141 c.1943G>A p.G648E Substitution - Missense 15:41818029-41818029 + 06-P2007 COSM4578220 c.1881C>T p.I627I Substitution - coding silent 15:41817712-41817712 + PD8995a COSM5782302 c.2581G>A p.G861S Substitution - Missense 15:41820913-41820913 + HCC76T COSM1608359 c.4422C>A p.G1474G Substitution - coding silent 15:41825331-41825331 + PCSI_0194_Pa_P COSM3377563 c.3497G>A p.R1166H Substitution - Missense 15:41823121-41823121 + T1764 COSM4700638 c.1747G>A p.A583T Substitution - Missense 15:41817423-41817423 + 2492702 COSM5599896 c.2767C>T p.H923Y Substitution - Missense 15:41821632-41821632 + LUAD_E00565 COSM389152 c.4399G>T p.G1467W Substitution - Missense 15:41825308-41825308 + PT46 COSM5929587 c.3343C>T p.P1115S Substitution - Missense 15:41822949-41822949 + TCGA-AR-A0U3-01 COSM5211365 c.436G>A p.A146T Substitution - Missense 15:41812065-41812065 + 169 COSM3729842 c.1332C>T p.S444S Substitution - coding silent 15:41815402-41815402 + ESO-0053 COSM961547 c.787C>T p.R263* Substitution - Nonsense 15:41813069-41813069 + ESCC_BICR_054T COSM5444199 c.2044G>A p.D682N Substitution - Missense 15:41818239-41818239 + HCC011T COSM5819991 c.1050T>G p.N350K Substitution - Missense 15:41814619-41814619 + PT19_2 COSM5900306 c.4168C>T p.P1390S Substitution - Missense 15:41824016-41824016 + T3118 COSM4700633 c.1130A>C p.K377T Substitution - Missense 15:41814681-41814681 + TCGA-G4-6302-01 COSM3690393 c.2886C>T p.N962N Substitution - coding silent 15:41821733-41821733 + RK308_C01 COSM3744599 c.1956G>A p.K652K Substitution - coding silent 15:41818042-41818042 + BD124T COSM5493264 c.3372G>A p.S1124S Substitution - coding silent 15:41822978-41822978 + 2492700 COSM5599895 c.2785C>T p.H929Y Substitution - Missense 15:41821632-41821632 + Pat_76_B COSM5849139 c.902C>T p.T301I Substitution - Missense 15:41813685-41813685 + TCGA-BR-4370-01 COSM4054603 c.3982C>T p.P1328S Substitution - Missense 15:41823812-41823812 + Pat_24_A COSM5849146 c.3709C>T p.R1237W Substitution - Missense 15:41823557-41823557 + TCGA-BR-8059-01 COSM4054583 c.673C>T p.L225L Substitution - coding silent 15:41812955-41812955 + BON-1 COSM5368216 c.2242C>T p.R748C Substitution - Missense 15:41818890-41818890 + TCGA-AB-2830-03 COSM1317795 c.402G>A p.K134K Substitution - coding silent 15:41812031-41812031 + MedB-1 COSM5621218 c.3620G>A p.R1207K Substitution - Missense 15:41823450-41823450 + TCGA-G9-6363-01 COSM1129211 c.1701T>C p.V567V Substitution - coding silent 15:41817025-41817025 + ccRCC-15 COSM1662696 c.2840G>C p.G947A Substitution - Missense 15:41821705-41821705 + TCGA-EE-A3JA-06 COSM3501126 c.1238C>T p.S413F Substitution - Missense 15:41815308-41815308 + TCGA-E2-A153-01 COSM5832896 c.3900C>T p.I1300I Substitution - coding silent 15:41823730-41823730 + pfg029T COSM1640232 c.3660A>T p.E1220D Substitution - Missense 15:41823508-41823508 + TCGA-EB-A551-01 COSM3501145 c.4084C>T p.P1362S Substitution - Missense 15:41823932-41823932 + T578 COSM4700643 c.2820C>A p.V940V Substitution - coding silent 15:41821667-41821667 + 587338 COSM1214547 c.889C>T p.R297C Substitution - Missense 15:41813690-41813690 + 93VU147T COSM4591124 c.2795G>A p.R932Q Substitution - Missense 15:41821642-41821642 + TCGA-BR-7703-01 COSM4054600 c.2452C>T p.R818* Substitution - Nonsense 15:41819621-41819621 + 10-104 COSM3736609 c.530C>T p.S177F Substitution - Missense 15:41812547-41812547 + TCGA-RP-A695-06 COSM4896979 c.1247C>T p.T416I Substitution - Missense 15:41815335-41815335 + TCGA-BH-A18G-01 COSM3816036 c.3086T>C p.I1029T Substitution - Missense 15:41822261-41822261 + PCSI_0194_Pa_P COSM3377562 c.3515G>A p.R1172H Substitution - Missense 15:41823121-41823121 + STC232 COSM5054280 c.3728G>A p.R1243Q Substitution - Missense 15:41823558-41823558 + T3417 COSM4700640 c.2068G>A p.V690M Substitution - Missense 15:41818281-41818281 + YUPAER COSM5383271 c.229_230CC>TT p.P77F Substitution - Missense 15:41810905-41810906 + PTC-7C COSM4148753 c.2474T>A p.M825K Substitution - Missense 15:41819643-41819643 + RK169_C01 COSM3700953 c.1366G>T p.D456Y Substitution - Missense 15:41815672-41815672 + TCGA-EJ-7125-01 COSM3672041 c.1363G>T p.G455W Substitution - Missense 15:41815651-41815651 + TCGA-16-0861-01 COSM3401722 c.1640C>T p.A547V Substitution - Missense 15:41816964-41816964 + TCGA-BR-4184-01 COSM4054587 c.757T>A p.S253T Substitution - Missense 15:41813039-41813039 + KPOPBR-34-T COSM5963297 c.3549C>A p.P1183P Substitution - coding silent 15:41823173-41823173 +

Mutation - CGAP UNIGENE CYTOBAND OMIM SNP Hs.513661 15q15.1

Mutation - IntOGen Mutated from(ref) Mutated to(alt) Consequence Type AA Mutation CDS Mutation Chr Pos Cancer A G Missense p.T707A c.2119A>G 15 42110725 UCEC A G Missense p.Y452C c.1355A>G 15 42107841 BRCA A G SpliceAcceptorSNV . c.2444-2A>G 15 42111791 HC A T 3-UTRSNV . c.4542+530A>T 15 42118161 HC A T Missense p.E1226D c.3678A>T 15 42115706 STAD A T Missense p.I674F c.2020A>T 15 42110413 HNSC A T Missense p.S333C c.997A>T 15 42105978 LUAD C - 3-UTRDeletion . c.4542+488delT 15 42118119 HC C A Missense p.A283D c.848C>A 15 42105829 PRAD C A Missense p.H520N c.1558C>A 15 42108803 RCCC C A Synonymous p.A1256A c.3768C>A 15 42115796 STAD CC TT Missense p.P77F c.229_230delinsTT 15 42103103 CM C - Frameshift p.R60Dfs*4 c.178delC 15 42092080 LUAD C G Missense p.R60G c.178C>G 15 42092084 CM C G Nonsense p.Y191* c.573C>G 15 42104788 UCEC C G Synonymous p.T351T c.1053C>G 15 42106802 CM C T IntronicSNV . c.1335+85C>T 15 42107688 CM C T IntronicSNV . c.2737-86C>T 15 42113696 CM C T IntronicSNV . c.637-6C>T 15 42105111 CM C T IntronicSNV . c.637-8C>T 15 42105109 CM C T IntronicSNV . c.820-24C>T 15 42105504 CM C T Missense p.A1037V c.3110C>T 15 42114483 UCEC C T Missense p.A553V c.1658C>T 15 42109162 GBM C T Missense p.H771Y c.2311C>T 15 42111445 BRCA C T Missense p.P1023L c.3068C>T 15 42114441 CM C T Missense p.P1241L c.3722C>T 15 42115750 CM C T Missense p.P1328S c.3982C>T 15 42116010 STAD C T Missense p.P1331S c.3991C>T 15 42116019 CM C T Missense p.P768L c.2303C>T 15 42111149 CM C T Missense p.P818S c.2452C>T 15 42111801 PAAD C T Missense p.P949S c.2845C>T 15 42113890 CM C T Missense p.S1099L c.3296C>T 15 42114839 CM C T Missense p.S1463L c.4388C>T 15 42117477 CM C T Missense p.S413F c.1238C>T 15 42107506 CM C T Missense p.S868F c.2603C>T 15 42113133 CM C T Missense p.S868F c.2603C>T 15 42113133 HNSC C T Missense p.S922F c.2765C>T 15 42113810 CM C T Missense p.T210I c.629C>T 15 42104844 CM C T Nonsense p.Q1418* c.4252C>T 15 42116702 HNSC C T Nonsense p.Q406* c.1216C>T 15 42107484 COREAD C T Nonsense p.R263* c.787C>T 15 42105267 ESCA C T Synonymous p.A1488A c.4464C>T 15 42117553 CM C T Synonymous p.A1505A c.4515C>T 15 42117604 HNSC C T Synonymous p.A349A c.1047C>T 15 42106796 LUSC C T Synonymous p.I1300I c.3900C>T 15 42115928 BRCA C T Synonymous p.I482I c.1446C>T 15 42107932 CM C T Synonymous p.L130L c.388C>T 15 42104215 UCEC C T Synonymous p.N1395N c.4185C>T 15 42116213 CM C T Synonymous p.N769N c.2307C>T 15 42111153 GBM C T Synonymous p.P399P c.1197C>T 15 42107465 GBM C T Synonymous p.P399P c.1197C>T 15 42107465 UCEC C T Synonymous p.R583R c.1749C>T 15 42109605 HNSC C T Synonymous p.R748R c.2244C>T 15 42111090 CM C T Synonymous p.S1159S c.3477C>T 15 42115281 THCA C T Synonymous p.S1259S c.3777C>T 15 42115805 CM C T Synonymous p.V582V c.1746C>T 15 42109602 CM G A IntronicSNV . c.269+13G>A 15 42103156 NSCLC G A IntronicSNV . c.637-37G>A 15 42105080 HC G A Missense p.A146T c.436G>A 15 42104263 BRCA G A Missense p.D472N c.1414G>A 15 42107900 BLCA G A Missense p.D58N c.172G>A 15 42092078 BLCA G A Missense p.E1391K c.4171G>A 15 42116199 HNSC G A Missense p.E187K c.559G>A 15 42104774 BRCA G A Missense p.E565K c.1693G>A 15 42109197 HNSC G A Missense p.G221D c.662G>A 15 42105142 STAD G A Missense p.R1243Q c.3728G>A 15 42115756 HNSC G A Missense p.R17K c.50G>A 15 42067523 HNSC G A Missense p.R743H c.2228G>A 15 42111074 COREAD G A Missense p.R743H c.2228G>A 15 42111074 GBM G A Missense p.R78Q c.233G>A 15 42103107 COREAD G A Missense p.R856H c.2567G>A 15 42113097 HNSC G A Missense p.V329I c.985G>A 15 42105966 COREAD G A SpliceAcceptorSNV . c.328-1G>A 15 42104154 HNSC G A Synonymous p.A340A c.1020G>A 15 42106769 GBM G A Synonymous p.K134K c.402G>A 15 42104229 AML G A Synonymous p.K808K c.2424G>A 15 42111558 HNSC G A Synonymous p.L74L c.222G>A 15 42103096 COREAD G A Synonymous p.T252T c.756G>A 15 42105236 STAD G C Missense p.E513D c.1539G>C 15 42108784 LUAD G C Missense p.G491R c.1471G>C 15 42107957 HNSC G C Missense p.G648A c.1943G>C 15 42110227 HNSC G C Synonymous p.S889S c.2667G>C 15 42113197 BRCA G - Frameshift p.E396Rfs*6 c.1186delG 15 42106934 COREAD G T IntronicSNV . c.3333-81G>T 15 42115056 CM G T Missense p.D420Y c.1258G>T 15 42107526 LUAD G T Missense p.R53I c.158G>T 15 42092064 BLCA G T Missense p.R918L c.2753G>T 15 42113798 BRCA G T SpliceDonorSNV . c.1922+1G>T 15 42109934 LUSC G T Synonymous p.G554G c.1662G>T 15 42109166 LUAD T A Missense p.L494Q c.1481T>A 15 42107967 RCCC T C Synonymous p.G659G c.1977T>C 15 42110261 STAD T G Missense p.S6A c.16T>G 15 42067489 GBM T G Synonymous p.T907T c.2721T>G 15 42113251 COREAD