ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-D01603 KLHL23 SNP Missense_Mutation 2 170592527 G A 34 100 LUAD LUAD-RT-S01840 KLHL23 SNP Splice_site 2 170606244 T A 63 48 LUAD LUAD-S01315 KLHL23 SNP Missense_Mutation 2 170606024 G C 45 83 LUAD LUAD-YINHD KLHL23 SNP Missense_Mutation 2 170605994 A G 4 75 LUAD LUAD_E00565 KLHL23 SNP Missense_Mutation 2 170592692 G A 45 100 MEL MEL-JWCI-WGS-7 KLHL23 SNP Missense_Mutation 2 170592285 C T 30 88 MEL MEL-JWCI-WGS-7 KLHL23 SNP Missense_Mutation 2 170598026 A C 8 55 LUAD TCGA-05-4398 KLHL23 SNP Silent 2 170592412 A T 5 59 LUSC TCGA-18-5592 KLHL23 SNP Missense_Mutation 2 170591838 G T 33 79 LUSC TCGA-34-2596 KLHL23 SNP Missense_Mutation 2 170592599 A T 7 64 LUSC TCGA-66-2771 KLHL23 SNP Missense_Mutation 2 170592730 G C 45 100 UCEC TCGA-A5-A0VP KLHL23 SNP Missense_Mutation 2 170592350 T C 57 93 CRC TCGA-AA-3977 KLHL23 SNP Missense_Mutation 2 170592688 C A 32 63 CRC TCGA-AA-3984 KLHL23 SNP Silent 2 170605954 G A 40 43 CRC TCGA-AA-A00N KLHL23 SNP Missense_Mutation 2 170592269 G A 37 87 CRC TCGA-AA-A010 KLHL23 SNP Nonsense_Mutation 2 170592044 G T 33 100 CRC TCGA-AA-A01P KLHL23 SNP Missense_Mutation 2 170606039 G T 34 77 AML TCGA-AB-2863 KLHL23 SNP Silent 2 170591818 C T 22 49 CRC TCGA-AG-A002 KLHL23 SNP Missense_Mutation 2 170592252 G T 33 70 UCEC TCGA-AP-A0LM KLHL23 SNP Missense_Mutation 2 170591740 A C 1 55 UCEC TCGA-B5-A11E KLHL23 SNP Missense_Mutation 2 170592000 G A 37 78 UCEC TCGA-B5-A11N KLHL23 SNP Missense_Mutation 2 170592003 G T 33 100 BRCA TCGA-BH-A0AV KLHL23 SNP Missense_Mutation 2 170592167 C G 31 86 UCEC TCGA-BS-A0TI KLHL23 SNP Missense_Mutation 2 170592281 C T 23 58 UCEC TCGA-BS-A0UF KLHL23 SNP Missense_Mutation 2 170598005 G T 37 100 UCEC TCGA-BS-A0UV KLHL23 SNP Missense_Mutation 2 170592208 T G 63 51 BRCA TCGA-C8-A131 KLHL23 SNP Missense_Mutation 2 170592266 A C 6 78 HNSC TCGA-CN-5356 KLHL23 SNP Missense_Mutation 2 170598005 G A 37 100 HNSC TCGA-CQ-5326 KLHL23 SNP Missense_Mutation 2 170592202 C G 29 52 HNSC TCGA-CR-7367 KLHL23 SNP Missense_Mutation 2 170592711 G T 47 100 HNSC TCGA-CV-6948 KLHL23 SNP Missense_Mutation 2 170591601 T C 62 89 UCEC TCGA-D1-A103 KLHL23 SNP Missense_Mutation 2 170592597 C A 26 100 UCEC TCGA-D1-A167 KLHL23 SNP Nonsense_Mutation 2 170597966 G T 35 100 UCEC TCGA-D1-A17Q KLHL23 SNP Missense_Mutation 2 170592168 G A 37 100