ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-5V8LT KLHDC8B SNP Missense_Mutation 3 49213124 C T 23 95 LUAD LUAD-CHTN-MAD06-00668 KLHDC8B SNP Silent 3 49210250 C A 21 53 LUAD TCGA-05-5425 KLHDC8B SNP Missense_Mutation 3 49212227 G C 35 72 LUAD TCGA-17-Z055 KLHDC8B DEL Frame_Shift_Del 3 49212336 C - 26 98 CRC TCGA-AA-3818 KLHDC8B SNP Silent 3 49213087 G A 42 67 CRC TCGA-AA-3864 KLHDC8B SNP Silent 3 49210331 A T 10 51 UCEC TCGA-AP-A059 KLHDC8B SNP Silent 3 49212320 C A 26 54 UCEC TCGA-AP-A0LG KLHDC8B SNP Silent 3 49213142 C T 32 65 UCEC TCGA-B5-A0JY KLHDC8B SNP Missense_Mutation 3 49212205 C A 28 87 BRCA TCGA-BH-A0BG KLHDC8B SNP Missense_Mutation 3 49211701 G A 43 100 KIRC TCGA-BP-4169 KLHDC8B SNP Silent 3 49210262 C T 26 58 KIRC TCGA-BP-5182 KLHDC8B SNP Missense_Mutation 3 49212294 G A 45 87 UCEC TCGA-BS-A0UV KLHDC8B SNP Silent 3 49211826 C A 32 98 BRCA TCGA-C8-A12W KLHDC8B SNP Missense_Mutation 3 49212375 G C 48 81 HNSC TCGA-CV-5440 KLHDC8B SNP Missense_Mutation 3 49210467 G A 45 57 HNSC TCGA-CV-6941 KLHDC8B DEL Frame_Shift_Del 3 49213226 G - 47 71 UCEC TCGA-D1-A103 KLHDC8B SNP Silent 3 49210370 G A 38 42 UCEC TCGA-D1-A103 KLHDC8B SNP Missense_Mutation 3 49210567 C A 20 69 BLCA TCGA-DK-A2I2 KLHDC8B SNP Missense_Mutation 3 49213182 C T 26 81 BLCA TCGA-DK-A3IT KLHDC8B SNP Missense_Mutation 3 49212384 T G 60 89