ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-105 BAIAP2 SNP Missense_Mutation 17 79060254 G C 33 65 ESO ESO-327 BAIAP2 SNP Splice_site 17 79077707 C T 27 64 LUAD LUAD-CHTN-MAD06-00668 BAIAP2 SNP Missense_Mutation 17 79073742 C G 29 75 LUAD LUAD-CHTN-MAD06-00668 BAIAP2 SNP Silent 17 79077493 G T 39 16 MED MD-280 BAIAP2 SNP Missense_Mutation 17 79077369 C T 23 97 MEL MEL-Ma-Mel-65 BAIAP2 SNP Missense_Mutation 17 79077887 C T 22 71 MEL MEL-Ma-Mel-76 BAIAP2 SNP Missense_Mutation 17 79077480 C T 26 83 MM MM-0551 BAIAP2 SNP Missense_Mutation 17 79077330 C T 23 97 LUSC TCGA-22-4595 BAIAP2 SNP Silent 17 79082295 G A 38 12 GBM TCGA-41-3392 BAIAP2 SNP Silent 17 79080620 C T 19 51 LUAD TCGA-49-4514 BAIAP2 SNP Silent 17 79058648 G A 33 68 LUSC TCGA-51-4080 BAIAP2 SNP Missense_Mutation 17 79080670 A T 7 58 LUAD TCGA-55-6712 BAIAP2 SNP Missense_Mutation 17 79060372 G A 41 95 LUSC TCGA-66-2785 BAIAP2 SNP Missense_Mutation 17 79077806 A G 5 61 LUAD TCGA-91-6829 BAIAP2 SNP Missense_Mutation 17 79090043 G A 38 31 CRC TCGA-AA-3956 BAIAP2 INS Frame_Shift_Ins 17 79089622 - C 46 68 CRC TCGA-AA-3984 BAIAP2 SNP Silent 17 79031742 C T 27 49 CRC TCGA-AA-A01R BAIAP2 SNP Silent 17 79060365 G A 39 32 CRC TCGA-AG-3586 BAIAP2 SNP Missense_Mutation 17 79027481 A G 7 87 UCEC TCGA-AP-A0LM BAIAP2 SNP Missense_Mutation 17 79073794 G A 38 96 UCEC TCGA-AX-A0J0 BAIAP2 SNP Splice_Site 17 79031768 G C 44 91 UCEC TCGA-B5-A0JZ BAIAP2 SNP Missense_Mutation 17 79058634 G A 33 81 UCEC TCGA-B5-A11E BAIAP2 SNP Missense_Mutation 17 79031759 A C 1 85 UCEC TCGA-BS-A0TA BAIAP2 SNP Missense_Mutation 17 79073809 C T 27 52 KIRC TCGA-CJ-4913 BAIAP2 SNP Silent 17 79027521 G A 33 72 HNSC TCGA-CN-4740 BAIAP2 SNP Silent 17 79058642 C T 32 49 HNSC TCGA-CQ-7068 BAIAP2 SNP Silent 17 79073793 C T 23 31 UCEC TCGA-D1-A177 BAIAP2 SNP Silent 17 79080548 G A 46 52 UCEC TCGA-D1-A17Q BAIAP2 SNP Silent 17 79073733 C T 31 36 UCEC TCGA-D1-A17Q BAIAP2 SNP Missense_Mutation 17 79079896 C A 32 58