ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0071 PPP2R5C SNP Silent 14 102368178 A G 2 55 LUAD LUAD-B00859 PPP2R5C SNP Missense_Mutation 14 102349884 A G 4 90 LUAD LUAD-CHTN-MAD06-00678 PPP2R5C SNP Missense_Mutation 14 102323129 A T 3 54 LUAD LUAD-LIP77 PPP2R5C SNP Nonsense_Mutation 14 102348564 G T 41 98 MEL ME009 PPP2R5C SNP Missense_Mutation 14 102391502 C T 23 76 MEL MEL-JWCI-WGS-22 PPP2R5C SNP Missense_Mutation 14 102391580 G A 37 84 PRAD PR-1043 PPP2R5C SNP Nonsense_Mutation 14 102348516 C T 31 65 OV TCGA-13-1507 PPP2R5C SNP Missense_Mutation 14 102384182 T G 58 62 LUAD TCGA-17-Z012 PPP2R5C SNP Missense_Mutation 14 102276305 G A 34 74 LUSC TCGA-18-3409 PPP2R5C SNP Missense_Mutation 14 102372829 C T 30 98 LUSC TCGA-18-3409 PPP2R5C SNP Missense_Mutation 14 102375971 G T 33 66 LUSC TCGA-22-4604 PPP2R5C SNP Missense_Mutation 14 102378761 G A 39 100 LUSC TCGA-37-3789 PPP2R5C SNP Missense_Mutation 14 102276371 G A 37 98 LUSC TCGA-60-2698 PPP2R5C SNP Missense_Mutation 14 102391487 G C 33 97 LUSC TCGA-60-2713 PPP2R5C SNP Missense_Mutation 14 102375969 G C 41 100 CRC TCGA-AA-3947 PPP2R5C SNP Nonsense_Mutation 14 102384282 C T 29 83 CRC TCGA-AA-3984 PPP2R5C SNP Missense_Mutation 14 102359423 C A 32 100 CRC TCGA-AG-A002 PPP2R5C SNP Missense_Mutation 14 102359423 C A 32 100 UCEC TCGA-AP-A051 PPP2R5C SNP Missense_Mutation 14 102372806 C T 27 98 UCEC TCGA-AP-A056 PPP2R5C SNP Nonsense_Mutation 14 102348516 C T 31 65 UCEC TCGA-AP-A056 PPP2R5C SNP Silent 14 102372814 C T 32 66 UCEC TCGA-AP-A0LM PPP2R5C SNP Missense_Mutation 14 102276296 A G 1 63 BRCA TCGA-AR-A0U2 PPP2R5C SNP Splice_Site 14 102384167 G A 36 95 UCEC TCGA-AX-A060 PPP2R5C SNP Missense_Mutation 14 102348535 C A 30 98 UCEC TCGA-B5-A11E PPP2R5C SNP Silent 14 102391579 C T 23 51 UCEC TCGA-BG-A0MQ PPP2R5C SNP Missense_Mutation 14 102391575 G T 35 97 HNSC TCGA-CV-6954 PPP2R5C SNP Missense_Mutation 14 102384193 C T 18 54 HNSC TCGA-CV-6962 PPP2R5C SNP Missense_Mutation 14 102391561 G C 47 97 UCEC TCGA-D1-A16F PPP2R5C SNP Silent 14 102384272 C T 19 51 UCEC TCGA-D1-A16Y PPP2R5C SNP Missense_Mutation 14 102323067 C T 19 87 UCEC TCGA-D1-A16Y PPP2R5C SNP Missense_Mutation 14 102349628 C T 32 84