ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-1096 LBX1 SNP Silent 10 102987147 C T 31 54 LUAD LUAD-B00915 LBX1 SNP Missense_Mutation 10 102987496 C A 31 98 LUAD LUAD-RT-S01707 LBX1 SNP Missense_Mutation 10 102988563 T G 63 66 LUAD LUAD-S01468 LBX1 SNP Splice_site 10 102987548 C A 24 86 MEL MEL-JWCI-WGS-25 LBX1 SNP Missense_Mutation 10 102987421 G A 41 85 MM MM-0492 LBX1 SNP Silent 10 102988477 T G 59 48 NB NB-1956 LBX1 SNP Silent 10 102987345 C T 26 59 LUAD TCGA-05-4396 LBX1 SNP Missense_Mutation 10 102987328 C A 23 87 LUAD TCGA-17-Z031 LBX1 SNP Missense_Mutation 10 102987515 G T 46 73 LUAD TCGA-17-Z046 LBX1 SNP Missense_Mutation 10 102987397 G A 38 100 LUSC TCGA-18-3414 LBX1 SNP Silent 10 102987414 G A 39 52 GBM TCGA-27-2523 LBX1 SNP Silent 10 102987489 C T 27 40 LUSC TCGA-37-4141 LBX1 SNP Silent 10 102987051 G A 40 67 LUSC TCGA-60-2724 LBX1 SNP Missense_Mutation 10 102987419 G A 43 100 CRC TCGA-AA-3977 LBX1 SNP Missense_Mutation 10 102987347 G A 37 100 CRC TCGA-AG-A002 LBX1 SNP Missense_Mutation 10 102987347 G A 37 100 UCEC TCGA-AP-A0LM LBX1 SNP Silent 10 102988471 C T 27 51 BRCA TCGA-C8-A26W LBX1 SNP Missense_Mutation 10 102987344 G T 38 74 HNSC TCGA-CR-6488 LBX1 SNP Missense_Mutation 10 102987175 C T 26 54 HNSC TCGA-CV-6938 LBX1 SNP Silent 10 102988336 G C 33 91