ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62624 GNB4 SNP Nonsense 3 179131518 G T 45 100 HNSC HN_63080 GNB4 SNP Synonymous 3 179123180 T C 50 40 LUAD LUAD-RT-S01810 GNB4 SNP Missense_Mutation 3 179132734 T C 49 51 MEL MEL-JWCI-WGS-3 GNB4 SNP Missense_Mutation 3 179131371 C G 32 88 MEL MEL-JWCI-WGS-31 GNB4 SNP Missense_Mutation 3 179132783 G A 43 100 PRAD PR-00-160 GNB4 SNP Silent 3 179131259 G T 37 86 GBM TCGA-12-0619 GNB4 INS Splice_site 3 179137188 - G 55 78 LUSC TCGA-21-1070 GNB4 SNP Missense_Mutation 3 179119032 G T 33 96 LUSC TCGA-22-5478 GNB4 SNP Missense_Mutation 3 179123052 C A 20 87 LUSC TCGA-46-3769 GNB4 SNP Missense_Mutation 3 179131506 G A 36 87 LUAD TCGA-49-4486 GNB4 SNP Missense_Mutation 3 179132738 G C 33 100 CRC TCGA-AA-3516 GNB4 SNP Missense_Mutation 3 179143946 G A 38 68 CRC TCGA-AA-3856 GNB4 SNP Nonsense_Mutation 3 179134312 A C 13 92 CRC TCGA-AA-3973 GNB4 INS Splice_site 3 179143987 - T 8 91 CRC TCGA-AA-A00N GNB4 SNP Missense_Mutation 3 179132751 C T 30 100 CRC TCGA-AG-3902 GNB4 SNP Silent 3 179134313 A G 4 62 UCEC TCGA-AP-A059 GNB4 SNP Silent 3 179138686 C T 27 28 UCEC TCGA-AX-A0J0 GNB4 SNP Missense_Mutation 3 179123026 C T 31 100 UCEC TCGA-B5-A0JY GNB4 SNP Missense_Mutation 3 179137238 A G 7 92 UCEC TCGA-BS-A0UF GNB4 SNP Missense_Mutation 3 179143986 C A 29 99 BLCA TCGA-BT-A2LB GNB4 SNP Silent 3 179119064 T C 61 51 HNSC TCGA-CN-4723 GNB4 SNP Missense_Mutation 3 179123134 C G 29 86 UCEC TCGA-D1-A15X GNB4 SNP Silent 3 179132797 G A 35 50 UCEC TCGA-D1-A174 GNB4 SNP Missense_Mutation 3 179137245 G A 40 86