ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-1 PLA2G12B SNP Silent 10 74695387 C T 24 51 LUAD TCGA-05-4396 PLA2G12B SNP Missense_Mutation 10 74714268 C A 22 94 OV TCGA-13-1494 PLA2G12B SNP Missense_Mutation 10 74702417 G A 47 77 LUAD TCGA-17-Z023 PLA2G12B SNP Missense_Mutation 10 74714335 G C 37 51 OV TCGA-25-2392 PLA2G12B SNP Silent 10 74701081 G A 46 59 LUAD TCGA-50-6590 PLA2G12B SNP Missense_Mutation 10 74714370 G T 35 63 BRCA TCGA-A2-A0EO PLA2G12B SNP Silent 10 74714297 G A 36 58 BRCA TCGA-A8-A094 PLA2G12B SNP Silent 10 74702434 G A 41 60 CRC TCGA-AA-A01P PLA2G12B SNP Silent 10 74714399 C A 22 51 AML TCGA-AB-2863 PLA2G12B SNP Splice_site 10 74714445 C A 24 54 UCEC TCGA-AP-A059 PLA2G12B SNP Missense_Mutation 10 74700957 G A 38 70 UCEC TCGA-AX-A0J1 PLA2G12B SNP Silent 10 74695492 G T 35 52 UCEC TCGA-AX-A0J1 PLA2G12B SNP Splice_Site 10 74700926 C T 18 96 UCEC TCGA-B5-A11E PLA2G12B SNP Silent 10 74714297 G A 36 58 UCEC TCGA-BG-A0MQ PLA2G12B SNP Missense_Mutation 10 74714325 C T 23 73 UCEC TCGA-D1-A167 PLA2G12B SNP Nonsense_Mutation 10 74714386 G A 45 78 HNSC TCGA-IQ-7630 PLA2G12B SNP Missense_Mutation 10 74700977 G C 37 73