ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-YINHD CST6 SNP Silent 11 65780865 G A 33 45 MEL ME002 CST6 SNP Silent 11 65779527 G A 37 46 MEL MEL-Ma-Mel-67 CST6 SNP Silent 11 65780320 C T 30 77 OV TCGA-23-2079 CST6 SNP Silent 11 65780321 C T 24 56 LUSC TCGA-66-2773 CST6 SNP Missense_Mutation 11 65779526 C G 31 52 AML TCGA-AB-2806 CST6 SNP Missense_Mutation 11 65780306 G C 39 77 CRC TCGA-AG-3587 CST6 SNP Missense_Mutation 11 65780352 G A 38 52 UCEC TCGA-BS-A0UF CST6 SNP Missense_Mutation 11 65780850 G T 34 57