ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-22 TM4SF18 SNP Nonsense_Mutation 3 149042728 G A 47 82 MEL MEL-Ma-Mel-114 TM4SF18 SNP Missense_Mutation 3 149042688 G A 34 58 GBM TCGA-06-0195 TM4SF18 SNP Silent 3 149051122 C A 27 35 OV TCGA-13-1512 TM4SF18 SNP Missense_Mutation 3 149042743 C T 25 62 LUSC TCGA-60-2713 TM4SF18 SNP Missense_Mutation 3 149048162 G T 48 42 UCEC TCGA-AP-A056 TM4SF18 SNP Missense_Mutation 3 149048185 G T 33 64 UCEC TCGA-AX-A063 TM4SF18 SNP Missense_Mutation 3 149048191 T C 60 58 UCEC TCGA-B5-A0JY TM4SF18 SNP Silent 3 149040145 G T 47 56 HNSC TCGA-CR-6484 TM4SF18 SNP Silent 3 149039271 G A 45 54