ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B01811 CSN2 SNP Missense_Mutation 4 70823069 G T 47 62 LUAD LUAD-F00162 CSN2 SNP Silent 4 70823214 C T 28 42 MEL ME043 CSN2 SNP Missense_Mutation 4 70823207 G A 43 51 MEL MEL-13447 CSN2 SNP Missense_Mutation 4 70823510 C T 30 49 MEL MEL-13473 CSN2 SNP Missense_Mutation 4 70823305 G A 47 55 MEL MEL-JWCI-27 CSN2 SNP Missense_Mutation 4 70824775 C T 32 49 MEL MEL-JWCI-WGS-7 CSN2 SNP Missense_Mutation 4 70823407 G A 35 45 MEL MEL-Ma-Mel-36 CSN2 SNP Missense_Mutation 4 70823086 T G 63 44 MEL MEL-Ma-Mel-65 CSN2 SNP Silent 4 70823463 G A 37 36 GBM TCGA-06-0119 CSN2 SNP Missense_Mutation 4 70823297 G T 44 48 LUSC TCGA-18-3409 CSN2 SNP Missense_Mutation 4 70826673 A G 3 72 GBM TCGA-19-5955 CSN2 SNP Missense_Mutation 4 70823249 G T 46 53 GBM TCGA-41-3393 CSN2 SNP Nonstop_Mutation 4 70822070 A G 15 69 LUAD TCGA-44-2655 CSN2 SNP Missense_Mutation 4 70823356 G C 34 48 LUAD TCGA-44-2657 CSN2 SNP Missense_Mutation 4 70823420 G T 42 50 LUAD TCGA-64-5775 CSN2 SNP Missense_Mutation 4 70823408 G A 42 55 LUAD TCGA-64-5781 CSN2 SNP Missense_Mutation 4 70823494 G A 33 51 CRC TCGA-AA-3947 CSN2 SNP Silent 4 70823400 C A 21 56 CRC TCGA-AA-A00N CSN2 SNP Silent 4 70823463 G A 37 36 CRC TCGA-AG-A002 CSN2 SNP Missense_Mutation 4 70823339 T C 59 53 BRCA TCGA-AO-A1KS CSN2 SNP Silent 4 70823234 G A 33 53 UCEC TCGA-AP-A059 CSN2 SNP Silent 4 70823382 C T 28 48 UCEC TCGA-BS-A0UF CSN2 SNP Nonsense_Mutation 4 70823066 C A 32 51 HNSC TCGA-CN-6988 CSN2 DNP Missense_Mutation 4 70823387 GG TT 43 49 HNSC TCGA-CR-7402 CSN2 SNP Missense_Mutation 4 70823471 A T 15 53 UCEC TCGA-D1-A103 CSN2 SNP Nonsense_Mutation 4 70823066 C A 32 51