ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CRC CRC-0007 KAT2B SNP Synonymous 3 20161160 C T 19 47 CLL CW113 KAT2B SNP Silent 3 20161199 A G 10 48 ESO ESO-085 KAT2B SNP Missense_Mutation 3 20169022 C T 18 89 LUAD LUAD-RT-S01702 KAT2B SNP Missense_Mutation 3 20193886 G A 42 100 MEL MEL-JWCI-27 KAT2B SNP Silent 3 20153274 C T 30 65 MEL MEL-JWCI-WGS-12 KAT2B SNP Silent 3 20181718 C T 32 57 MEL MEL-JWCI-WGS-12 KAT2B SNP Missense_Mutation 3 20189905 G A 34 74 MM MM-0573 KAT2B SNP Missense_Mutation 3 20113948 C G 24 65 LUAD TCGA-05-4244 KAT2B SNP Missense_Mutation 3 20164279 G A 34 81 LUAD TCGA-05-4396 KAT2B SNP Missense_Mutation 3 20113931 G T 39 93 LUAD TCGA-05-4396 KAT2B SNP Missense_Mutation 3 20181816 C A 23 100 LUAD TCGA-17-Z045 KAT2B SNP Missense_Mutation 3 20164180 G T 45 89 LUSC TCGA-18-3409 KAT2B SNP Missense_Mutation 3 20178441 G T 41 100 OV TCGA-25-1627 KAT2B SNP Missense_Mutation 3 20136781 G A 48 70 LUSC TCGA-43-2578 KAT2B SNP Missense_Mutation 3 20136868 G T 33 100 LUSC TCGA-43-6143 KAT2B SNP Missense_Mutation 3 20082244 A G 11 79 LUAD TCGA-44-6775 KAT2B SNP Missense_Mutation 3 20082268 G A 46 84 LUSC TCGA-56-5898 KAT2B SNP Missense_Mutation 3 20142869 C T 23 88 LUSC TCGA-66-2773 KAT2B SNP Silent 3 20189783 C T 30 80 LUAD TCGA-67-3770 KAT2B SNP Splice_Site 3 20167606 G T 40 99 UCEC TCGA-A5-A0VP KAT2B SNP Missense_Mutation 3 20193899 G A 37 100 CRC TCGA-AA-3516 KAT2B SNP Silent 3 20113890 C T 23 48 CRC TCGA-AA-3977 KAT2B SNP Missense_Mutation 3 20156432 G A 41 84 CRC TCGA-AA-3977 KAT2B SNP Missense_Mutation 3 20181824 G A 33 100 CRC TCGA-AA-3977 KAT2B SNP Missense_Mutation 3 20187848 G A 37 88 CRC TCGA-AA-A00N KAT2B SNP Nonsense_Mutation 3 20167466 G T 45 100 CRC TCGA-AA-A00N KAT2B SNP Nonsense_Mutation 3 20167577 G T 33 100 CRC TCGA-AA-A00N KAT2B SNP Nonsense_Mutation 3 20181725 G T 33 100 AML TCGA-AB-2808 KAT2B SNP Missense_Mutation 3 20136845 G A 48 100 AML TCGA-AB-3008 KAT2B SNP Silent 3 20164251 G A 35 69 CRC TCGA-AG-A002 KAT2B SNP Nonsense_Mutation 3 20187847 C T 31 85 CRC TCGA-AG-A002 KAT2B SNP Missense_Mutation 3 20189935 G T 33 83 UCEC TCGA-AP-A056 KAT2B SNP Missense_Mutation 3 20187848 G A 37 88 UCEC TCGA-AP-A059 KAT2B SNP Missense_Mutation 3 20153107 G A 40 100 UCEC TCGA-AP-A0LM KAT2B SNP Missense_Mutation 3 20153174 G A 38 100 UCEC TCGA-AX-A0J0 KAT2B SNP Nonsense_Mutation 3 20142827 G T 33 100 UCEC TCGA-AX-A0J0 KAT2B SNP Missense_Mutation 3 20164214 G A 37 100 UCEC TCGA-AX-A0J0 KAT2B SNP Missense_Mutation 3 20187830 G T 33 100 UCEC TCGA-AX-A0J1 KAT2B SNP Missense_Mutation 3 20167452 G A 38 100 UCEC TCGA-B5-A11E KAT2B SNP Splice_Site 3 20142961 G A 44 100 UCEC TCGA-B5-A11E KAT2B SNP Nonsense_Mutation 3 20167577 G T 33 100 BRCA TCGA-BH-A0HP KAT2B SNP Silent 3 20161094 C A 29 76 KIRC TCGA-BP-4782 KAT2B SNP Missense_Mutation 3 20153227 A G 1 93 KIRC TCGA-BP-4971 KAT2B SNP Silent 3 20153265 C T 29 57 BLCA TCGA-BT-A0YX KAT2B SNP Missense_Mutation 3 20082225 C G 30 85 HNSC TCGA-CV-7414 KAT2B SNP Missense_Mutation 3 20181763 C G 29 61 UCEC TCGA-D1-A16Y KAT2B SNP Missense_Mutation 3 20141413 G T 33 62 UCEC TCGA-D1-A16Y KAT2B SNP Splice_Site 3 20167607 T C 57 91 UCEC TCGA-D1-A174 KAT2B SNP Missense_Mutation 3 20167452 G A 38 100 UCEC TCGA-D1-A17Q KAT2B SNP Missense_Mutation 3 20187830 G T 33 100 HNSC TCGA-D6-6516 KAT2B SNP Silent 3 20113935 T C 60 49 BRCA TCGA-D8-A1X6 KAT2B SNP Missense_Mutation 3 20167590 G A 39 99 BRCA TCGA-E2-A10C KAT2B SNP Silent 3 20167519 G T 45 57