ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-Ma-Mel-79 HMGB2 SNP Missense_Mutation 4 174254130 A G 2 91 LUAD TCGA-05-4396 HMGB2 SNP Missense_Mutation 4 174253366 C A 24 87 LUAD TCGA-05-4396 HMGB2 SNP Missense_Mutation 4 174254076 C A 21 85 LUAD TCGA-05-4396 HMGB2 SNP Splice_site 4 174254220 G T 39 77 LUAD TCGA-05-4396 HMGB2 SNP Missense_Mutation 4 174254772 C A 23 78 LUAD TCGA-17-Z053 HMGB2 SNP Silent 4 174254255 C G 30 53 LUSC TCGA-18-3407 HMGB2 SNP Missense_Mutation 4 174254762 C A 17 86 BRCA TCGA-A1-A0SF HMGB2 SNP Missense_Mutation 4 174254704 C T 30 100 UCEC TCGA-A5-A0GW HMGB2 SNP Silent 4 174253279 C T 24 45 CRC TCGA-AA-3984 HMGB2 SNP Missense_Mutation 4 174254253 T G 56 77 CRC TCGA-AG-A016 HMGB2 SNP Silent 4 174254768 G T 46 68 UCEC TCGA-AP-A054 HMGB2 SNP Splice_Site 4 174253970 A G 14 59 UCEC TCGA-AX-A05Z HMGB2 SNP Nonsense_Mutation 4 174254125 G T 34 62 UCEC TCGA-B5-A0JY HMGB2 SNP Nonsense_Mutation 4 174253272 C A 32 97 UCEC TCGA-BK-A0C9 HMGB2 SNP Missense_Mutation 4 174254247 T C 56 89 UCEC TCGA-BS-A0UV HMGB2 SNP Silent 4 174254717 C T 32 78 BLCA TCGA-BT-A20P HMGB2 SNP Missense_Mutation 4 174254073 C G 30 86 BRCA TCGA-C8-A274 HMGB2 SNP Missense_Mutation 4 174254097 C T 29 99 BLCA TCGA-CF-A1HR HMGB2 SNP Silent 4 174254744 G A 37 64 BLCA TCGA-CF-A3MH HMGB2 DEL In_Frame_Del 4 174253235 TCTTCA - 62 89 HNSC TCGA-CV-6961 HMGB2 SNP Silent 4 174254786 G A 44 65 HNSC TCGA-CV-7097 HMGB2 SNP Missense_Mutation 4 174254247 T C 56 89 UCEC TCGA-D1-A15X HMGB2 DEL In_Frame_Del 4 174253307 TTC - 60 51 BLCA TCGA-DK-A1A3 HMGB2 SNP Missense_Mutation 4 174254236 C A 25 86 BLCA TCGA-DK-A3IN HMGB2 SNP Silent 4 174254744 G A 37 64 BRCA TCGA-E2-A15O HMGB2 SNP Missense_Mutation 4 174254765 T A 64 48