ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-Ma-Mel-114 SC5DL SNP Missense_Mutation 11 121175158 G A 33 78 LUAD TCGA-05-4396 SC5DL SNP Missense_Mutation 11 121177872 C A 24 100 OV TCGA-13-0924 SC5DL SNP Silent 11 121177111 C T 31 44 LUSC TCGA-34-5927 SC5DL SNP Missense_Mutation 11 121175181 G C 45 52 LUAD TCGA-44-6145 SC5DL SNP Missense_Mutation 11 121177914 A T 14 79 LUAD TCGA-50-5930 SC5DL SNP Missense_Mutation 11 121174133 G T 40 53 LUAD TCGA-73-4677 SC5DL SNP Missense_Mutation 11 121174140 C T 21 87 LUAD TCGA-91-6829 SC5DL SNP Missense_Mutation 11 121174109 G C 33 100 CRC TCGA-AA-3821 SC5DL SNP Missense_Mutation 11 121178115 C T 23 97 CRC TCGA-AA-3977 SC5DL SNP Silent 11 121174258 C T 31 61 CRC TCGA-AA-A00N SC5DL SNP Missense_Mutation 11 121178026 C A 32 71 CRC TCGA-AG-3892 SC5DL SNP Missense_Mutation 11 121177986 T G 64 79 CRC TCGA-AG-A002 SC5DL SNP Missense_Mutation 11 121175083 G A 37 72 UCEC TCGA-AP-A051 SC5DL SNP Missense_Mutation 11 121174242 G T 34 59 UCEC TCGA-AX-A0J0 SC5DL SNP Missense_Mutation 11 121174203 T C 60 92 HNSC TCGA-BA-6872 SC5DL SNP Silent 11 121174255 C G 32 52 UCEC TCGA-BS-A0UV SC5DL SNP Nonsense_Mutation 11 121175082 C T 31 59 HNSC TCGA-CR-5249 SC5DL SNP Silent 11 121178029 T C 63 51 BLCA TCGA-DK-A1AC SC5DL SNP Missense_Mutation 11 121174160 G C 45 60 KIRC TCGA-EU-5904 SC5DL SNP Missense_Mutation 11 121175086 A T 11 92