ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-153 SLC7A5 SNP Missense_Mutation 16 87902970 T G 62 84 MEL ME033 SLC7A5 SNP Silent 16 87871538 G A 37 53 MEL MEL-JWCI-WGS-12 SLC7A5 SNP Silent 16 87902894 G A 43 51 MEL MEL-JWCI-WGS-12 SLC7A5 SNP Missense_Mutation 16 87902911 C G 31 62 MEL MEL-Ma-Mel-67 SLC7A5 SNP Silent 16 87873413 G T 45 77 MEL MEL-Ma-Mel-67 SLC7A5 SNP Silent 16 87902573 G A 37 94 GBM TCGA-06-0879 SLC7A5 SNP Missense_Mutation 16 87873313 C A 26 96 GBM TCGA-06-5858 SLC7A5 SNP Missense_Mutation 16 87873310 C T 19 82 LUSC TCGA-18-3406 SLC7A5 SNP Missense_Mutation 16 87902863 C A 19 93 LUAD TCGA-49-6742 SLC7A5 SNP Splice_site 16 87866630 G C 33 55 LUSC TCGA-66-2756 SLC7A5 SNP Silent 16 87874694 C G 25 59 CRC TCGA-AA-A01T SLC7A5 SNP Missense_Mutation 16 87866620 C T 19 78 UCEC TCGA-AP-A051 SLC7A5 SNP Missense_Mutation 16 87866581 T C 58 56 UCEC TCGA-B5-A0JY SLC7A5 SNP Silent 16 87872373 G A 37 53 UCEC TCGA-B5-A11E SLC7A5 SNP Silent 16 87868147 G A 37 53 UCEC TCGA-BG-A0M8 SLC7A5 SNP Missense_Mutation 16 87873324 G C 41 99 UCEC TCGA-BG-A0MQ SLC7A5 SNP Silent 16 87873425 C T 25 56 KIRC TCGA-CJ-4644 SLC7A5 SNP Silent 16 87885388 G A 39 43 KIRC TCGA-CJ-4886 SLC7A5 SNP Silent 16 87871508 G A 47 38 HNSC TCGA-CQ-5334 SLC7A5 SNP Missense_Mutation 16 87874057 C T 32 100 HNSC TCGA-CR-7368 SLC7A5 INS Frame_Shift_Ins 16 87885358 - A 41 57 UCEC TCGA-D1-A103 SLC7A5 SNP Missense_Mutation 16 87902836 C T 23 93 UCEC TCGA-D1-A15X SLC7A5 SNP Missense_Mutation 16 87902661 A G 10 86 UCEC TCGA-D1-A161 SLC7A5 SNP Missense_Mutation 16 87873316 C T 19 96 UCEC TCGA-D1-A174 SLC7A5 SNP Missense_Mutation 16 87868104 A G 3 78 BRCA TCGA-D8-A1JK SLC7A5 SNP Missense_Mutation 16 87874747 G C 33 75