ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62374 PLEKHB2 SNP Synonymous 2 131890540 G A 39 47 LUAD LUAD-B01024 PLEKHB2 SNP Splice_site 2 131904346 G T 35 52 LUAD LUAD-RT-S01813 PLEKHB2 SNP Missense_Mutation 2 131897835 G T 36 62 LUAD LUAD-S01357 PLEKHB2 SNP Missense_Mutation 2 132110622 C G 17 51 LUAD LUAD-S01467 PLEKHB2 SNP Missense_Mutation 2 131888326 C A 17 62 MM MM-0284 PLEKHB2 SNP Silent 2 131897769 T G 59 42 OV TCGA-13-1412 PLEKHB2 SNP Missense_Mutation 2 131904258 A T 16 79 OV TCGA-24-1422 PLEKHB2 SNP Missense_Mutation 2 131884288 C G 20 52 LUAD TCGA-49-6767 PLEKHB2 SNP Nonsense_Mutation 2 131883346 A T 9 84 LUAD TCGA-50-5941 PLEKHB2 SNP Missense_Mutation 2 131904333 T C 64 79 LUSC TCGA-60-2720 PLEKHB2 SNP Missense_Mutation 2 131897811 G T 42 41 LUAD TCGA-64-5775 PLEKHB2 SNP Missense_Mutation 2 132110713 G T 48 74 BRCA TCGA-A2-A04P PLEKHB2 SNP Missense_Mutation 2 131904268 C G 19 47 CRC TCGA-AA-3977 PLEKHB2 SNP Missense_Mutation 2 131883457 C T 23 76 UCEC TCGA-AP-A0LM PLEKHB2 SNP Splice_site 2 131883476 G A 39 66 UCEC TCGA-B5-A11E PLEKHB2 SNP Missense_Mutation 2 131897756 G A 43 66 KIRC TCGA-BP-4338 PLEKHB2 SNP Missense_Mutation 2 131883458 G A 38 91 UCEC TCGA-BS-A0UV PLEKHB2 SNP Nonsense_Mutation 2 131904260 C T 31 65 BLCA TCGA-C4-A0EZ PLEKHB2 SNP Silent 2 131904340 C T 32 63 BRCA TCGA-C8-A134 PLEKHB2 SNP Missense_Mutation 2 132110630 C T 19 53 HNSC TCGA-CV-7263 PLEKHB2 SNP Missense_Mutation 2 131890487 T C 54 71 UCEC TCGA-D1-A15W PLEKHB2 SNP Missense_Mutation 2 132110679 C A 27 61 UCEC TCGA-D1-A15X PLEKHB2 SNP Missense_Mutation 2 131883460 A G 6 71 BRCA TCGA-E2-A1IL PLEKHB2 SNP Missense_Mutation 2 131883435 G A 46 77