ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-805 KLHL5 SNP Missense_Mutation 4 39088271 G A 40 76 HNSC HN_0-046 KLHL5 SNP Missense 4 39098493 C G 17 100 LUAD LUAD-F00162 KLHL5 SNP Missense_Mutation 4 39116876 G T 48 100 LUAD LUAD-F00368 KLHL5 SNP Splice_Site 4 39098499 G T 44 99 LUAD LUAD-RT-S01700 KLHL5 SNP Missense_Mutation 4 39098477 G T 47 100 LUAD LUAD-YINHD KLHL5 SNP Missense_Mutation 4 39114656 G T 47 100 MEL MEL-JWCI-WGS-12 KLHL5 SNP Missense_Mutation 4 39064409 G A 41 61 MEL MEL-JWCI-WGS-24 KLHL5 SNP Missense_Mutation 4 39105081 C G 17 100 MM MM-0514 KLHL5 SNP Silent 4 39098458 T C 63 46 NB NB-3264 KLHL5 SNP Missense_Mutation 4 39109338 G A 36 87 LUAD TCGA-05-4396 KLHL5 SNP Silent 4 39114811 C A 23 38 GBM TCGA-06-0743 KLHL5 SNP Missense_Mutation 4 39116882 G A 43 100 GBM TCGA-06-5410 KLHL5 SNP Silent 4 39116788 C G 21 47 OV TCGA-13-0730 KLHL5 SNP Missense_Mutation 4 39114765 C T 19 100 LUSC TCGA-37-4135 KLHL5 SNP Silent 4 39064185 A G 8 66 LUSC TCGA-39-5031 KLHL5 SNP Missense_Mutation 4 39122658 G A 41 94 LUAD TCGA-44-2657 KLHL5 SNP Missense_Mutation 4 39116892 G T 41 100 LUAD TCGA-44-3918 KLHL5 DEL Frame_Shift_Del 4 39109334 G - 47 51 LUAD TCGA-49-4486 KLHL5 SNP Splice_Site 4 39082722 G C 33 100 LUSC TCGA-66-2768 KLHL5 SNP Nonsense_Mutation 4 39083642 C T 29 87 LUSC TCGA-85-6560 KLHL5 SNP Silent 4 39082828 G A 40 46 LUAD TCGA-91-6836 KLHL5 SNP Missense_Mutation 4 39064576 G C 39 86 UCEC TCGA-A5-A0GP KLHL5 SNP Missense_Mutation 4 39083717 C T 31 100 BRCA TCGA-A8-A093 KLHL5 SNP Missense_Mutation 4 39064478 G A 37 61 CRC TCGA-AA-3672 KLHL5 DEL Frame_Shift_Del 4 39077685 A - 13 69 CRC TCGA-AA-3955 KLHL5 SNP Missense_Mutation 4 39098386 G T 45 100 CRC TCGA-AA-3984 KLHL5 SNP Nonsense_Mutation 4 39064633 G T 45 86 CRC TCGA-AA-3984 KLHL5 SNP Missense_Mutation 4 39083717 C T 31 100 CRC TCGA-AA-A00N KLHL5 SNP Missense_Mutation 4 39083717 C T 31 100 CRC TCGA-AA-A010 KLHL5 SNP Missense_Mutation 4 39083717 C T 31 100 CRC TCGA-AA-A010 KLHL5 DEL Frame_Shift_Del 4 39114642 T - 56 91 AML TCGA-AB-2853 KLHL5 SNP Silent 4 39114766 G A 37 28 CRC TCGA-AG-A002 KLHL5 SNP Missense_Mutation 4 39064478 G A 37 61 CRC TCGA-AG-A002 KLHL5 SNP Missense_Mutation 4 39077652 T C 64 91 CRC TCGA-AG-A002 KLHL5 SNP Missense_Mutation 4 39088307 A C 1 54 CRC TCGA-AG-A02N KLHL5 SNP Missense_Mutation 4 39098493 C T 17 100 UCEC TCGA-AP-A056 KLHL5 SNP Missense_Mutation 4 39064252 G A 37 65 UCEC TCGA-AP-A056 KLHL5 SNP Nonsense_Mutation 4 39082796 G T 33 100 UCEC TCGA-AP-A056 KLHL5 SNP Missense_Mutation 4 39114672 C A 32 88 UCEC TCGA-AP-A0LM KLHL5 SNP Silent 4 39088137 G A 34 52 KIRC TCGA-B0-4837 KLHL5 SNP Missense_Mutation 4 39116919 C T 28 100 UCEC TCGA-B5-A11E KLHL5 SNP Silent 4 39064158 A G 14 52 UCEC TCGA-B5-A11E KLHL5 SNP Missense_Mutation 4 39088217 A G 10 93 HNSC TCGA-CN-6992 KLHL5 SNP Missense_Mutation 4 39122661 C G 28 94 KIRC TCGA-CZ-4863 KLHL5 SNP Missense_Mutation 4 39083717 C G 31 100 UCEC TCGA-D1-A16X KLHL5 SNP Missense_Mutation 4 39116783 G A 45 100 UCEC TCGA-D1-A17F KLHL5 SNP Silent 4 39064614 C T 25 59 BRCA TCGA-D8-A27T KLHL5 SNP Silent 4 39114838 A G 7 50 BLCA TCGA-DK-A2I4 KLHL5 SNP Nonsense_Mutation 4 39116803 G A 41 100 HNSC TCGA-HL-7533 KLHL5 SNP Missense_Mutation 4 39064535 C T 32 86