ttype patient gene classification type chr pos ref_allele newbase context65 cons46 DLBCL DLBCL-Ls1620 FGF20 SNP Missense_Mutation 8 16850771 T G 60 91 ESO ESO-805 FGF20 SNP Missense_Mutation 8 16850636 G T 47 85 LUAD LUAD-B00523 FGF20 SNP Missense_Mutation 8 16850671 C A 32 61 MEL MEL-JWCI-WGS-3 FGF20 SNP Missense_Mutation 8 16850681 G A 42 99 PRAD P09-649 FGF20 SNP Splice_site 8 16850824 C T 32 65 GBM TCGA-06-0190 FGF20 SNP Silent 8 16850701 G A 40 50 LUSC TCGA-18-3409 FGF20 SNP Silent 8 16850674 G A 47 55 LUAD TCGA-64-1676 FGF20 SNP Missense_Mutation 8 16850805 T A 51 62 CRC TCGA-AA-3984 FGF20 SNP Silent 8 16850782 C A 32 64 CRC TCGA-AG-A002 FGF20 SNP Missense_Mutation 8 16850811 C T 31 99 KIRC TCGA-B0-4838 FGF20 SNP Missense_Mutation 8 16850793 G C 46 85 HNSC TCGA-CN-4723 FGF20 SNP Silent 8 16850803 G T 33 58 HNSC TCGA-CV-6441 FGF20 SNP Missense_Mutation 8 16850824 C G 32 65 BLCA TCGA-FD-A3N5 FGF20 SNP Silent 8 16859521 G A 37 53