ttype patient gene classification type chr pos ref_allele newbase context65 cons46 CRC CRC-0002 PRKAR2B SNP Missense 7 106797436 C T 31 46 ESO ESO-153 PRKAR2B SNP Silent 7 106797642 A G 3 48 LUAD LUAD-S01405 PRKAR2B SNP Missense_Mutation 7 106791406 G A 46 100 MEL ME009 PRKAR2B SNP Silent 7 106793636 G A 45 54 OV TCGA-13-1504 PRKAR2B SNP Missense_Mutation 7 106786832 G A 37 100 GBM TCGA-14-1450 PRKAR2B SNP Splice_site 7 106786905 T G 63 92 LUSC TCGA-18-4083 PRKAR2B SNP Missense_Mutation 7 106786829 G T 39 100 LUSC TCGA-22-4604 PRKAR2B SNP Silent 7 106781375 T G 59 48 LUSC TCGA-33-4583 PRKAR2B SNP Silent 7 106786783 T C 51 51 LUSC TCGA-39-5037 PRKAR2B SNP Nonsense_Mutation 7 106710740 C T 23 60 LUSC TCGA-60-2715 PRKAR2B SNP Missense_Mutation 7 106791406 G T 46 100 CRC TCGA-AA-3947 PRKAR2B SNP Nonsense_Mutation 7 106797673 C T 31 68 CRC TCGA-AA-A00N PRKAR2B SNP Missense_Mutation 7 106797436 C T 31 46 CRC TCGA-AG-3892 PRKAR2B SNP Missense_Mutation 7 106710753 G A 40 71 UCEC TCGA-AP-A051 PRKAR2B SNP Splice_site 7 106781398 G T 35 86 UCEC TCGA-AP-A059 PRKAR2B SNP Silent 7 106781369 C T 19 51 BRCA TCGA-AR-A0TP PRKAR2B SNP Missense_Mutation 7 106786812 A G 12 91 KIRC TCGA-B0-4712 PRKAR2B SNP Splice_site 7 106799894 C G 25 74 UCEC TCGA-BS-A0UV PRKAR2B SNP Nonsense_Mutation 7 106710740 C T 23 60 UCEC TCGA-BS-A0UV PRKAR2B SNP Nonsense_Mutation 7 106768681 C T 29 88 HNSC TCGA-CV-6952 PRKAR2B SNP Missense_Mutation 7 106781346 G A 41 100 HNSC TCGA-CV-7418 PRKAR2B SNP Missense_Mutation 7 106781395 A T 12 92 UCEC TCGA-D1-A16X PRKAR2B SNP Nonsense_Mutation 7 106797673 C T 31 68 BLCA TCGA-G2-A2EO PRKAR2B SNP Missense_Mutation 7 106797459 G C 33 100