ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B01246 RTN4RL1 SNP Missense_Mutation 17 1841064 C G 30 70 MEL MEL-JWCI-WGS-25 RTN4RL1 SNP Missense_Mutation 17 1840755 A C 3 93 MEL MEL-JWCI-WGS-25 RTN4RL1 SNP Silent 17 1841079 G A 34 65 MEL MEL-JWCI-WGS-34 RTN4RL1 SNP Silent 17 1839940 G A 45 51 MEL MEL-Ma-Mel-63 RTN4RL1 SNP Silent 17 1839853 C T 23 50 MEL MEL-Ma-Mel-67 RTN4RL1 SNP Missense_Mutation 17 1840839 G A 43 85 MM MM-0499 RTN4RL1 SNP Missense_Mutation 17 1840356 C T 23 85 MEL Mel_BRAFi_02_PRE RTN4RL1 DNP Missense_Mutation 17 1840959 GG AA 43 100 LUAD TCGA-17-Z031 RTN4RL1 SNP Missense_Mutation 17 1840809 C T 30 100 LUSC TCGA-60-2712 RTN4RL1 DEL Frame_Shift_Del 17 1840292 C - 26 85 BRCA TCGA-A7-A0CE RTN4RL1 SNP Nonsense_Mutation 17 1840864 G C 36 66 CRC TCGA-AA-3710 RTN4RL1 SNP Missense_Mutation 17 1840206 A G 7 78 CRC TCGA-AA-3715 RTN4RL1 SNP Missense_Mutation 17 1840329 C T 27 84 CRC TCGA-AA-3966 RTN4RL1 SNP Missense_Mutation 17 1840731 C T 27 86 AML TCGA-AB-2959 RTN4RL1 SNP Missense_Mutation 17 1840686 C T 19 63 BRCA TCGA-AN-A0XP RTN4RL1 SNP Silent 17 1839853 C T 23 50 UCEC TCGA-B5-A0K8 RTN4RL1 SNP Silent 17 1840681 A G 5 43 KIRC TCGA-BP-4963 RTN4RL1 SNP Silent 17 1840903 G T 39 45 UCEC TCGA-BS-A0UL RTN4RL1 SNP Silent 17 1840573 G A 40 46 HNSC TCGA-CR-6478 RTN4RL1 SNP Missense_Mutation 17 1840605 C T 30 86 HNSC TCGA-CR-7383 RTN4RL1 SNP Missense_Mutation 17 1840355 C A 26 72 HNSC TCGA-CR-7402 RTN4RL1 DEL Frame_Shift_Del 17 1841024 CA - 25 100 UCEC TCGA-D1-A103 RTN4RL1 SNP Silent 17 1840633 G A 37 41 UCEC TCGA-D1-A17D RTN4RL1 SNP Missense_Mutation 17 1841096 C T 17 58