ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0033 P4HTM SNP Silent 3 49044229 G C 42 52 MEL ME009 P4HTM SNP Missense_Mutation 3 49044156 G A 43 95 MEL ME020 P4HTM DNP Missense_Mutation 3 49044215 CC TT 22 95 MEL MEL-Ma-Mel-65 P4HTM SNP Silent 3 49042327 C T 31 47 LUAD TCGA-05-4410 P4HTM SNP Missense_Mutation 3 49044234 C A 27 60 LUAD TCGA-05-4427 P4HTM SNP Missense_Mutation 3 49044257 C A 23 88 GBM TCGA-06-5858 P4HTM SNP Missense_Mutation 3 49043241 G A 40 98 GBM TCGA-12-3653 P4HTM SNP Missense_Mutation 3 49042445 G A 34 68 OV TCGA-13-1483 P4HTM SNP Missense_Mutation 3 49042491 C A 22 50 LUSC TCGA-18-3421 P4HTM SNP Silent 3 49044337 C G 32 56 LUSC TCGA-18-5595 P4HTM SNP Missense_Mutation 3 49039978 G A 33 91 LUSC TCGA-18-5595 P4HTM SNP Missense_Mutation 3 49043509 G A 41 72 LUSC TCGA-18-5595 P4HTM SNP Missense_Mutation 3 49043512 G T 45 61 LUAD TCGA-35-3621 P4HTM INS Frame_Shift_Ins 3 49027897 - TG 24 54 LUSC TCGA-43-6770 P4HTM SNP Missense_Mutation 3 49044195 A G 2 88 LUAD TCGA-44-2659 P4HTM SNP Missense_Mutation 3 49027918 G A 42 89 LUAD TCGA-44-3396 P4HTM SNP Silent 3 49042348 G T 46 52 LUAD TCGA-44-3396 P4HTM SNP Missense_Mutation 3 49042350 A C 7 89 CRC TCGA-AG-A02N P4HTM SNP Silent 3 49039998 C T 19 57 UCEC TCGA-AP-A059 P4HTM SNP Silent 3 49028289 G A 34 59 UCEC TCGA-AP-A059 P4HTM SNP Missense_Mutation 3 49042505 C T 26 48 UCEC TCGA-AP-A0LM P4HTM SNP Missense_Mutation 3 49039994 T C 51 84 UCEC TCGA-AP-A0LM P4HTM SNP Splice_site 3 49040029 G A 39 90 UCEC TCGA-AP-A0LM P4HTM SNP Missense_Mutation 3 49044306 A G 10 77 BRCA TCGA-AR-A1AJ P4HTM SNP Missense_Mutation 3 49038967 A C 11 77 UCEC TCGA-AX-A0J1 P4HTM SNP Silent 3 49042339 C T 27 38 UCEC TCGA-B5-A11R P4HTM SNP Missense_Mutation 3 49044152 C T 25 95 HNSC TCGA-BA-4077 P4HTM SNP Missense_Mutation 3 49040007 C G 29 61 BLCA TCGA-BT-A20T P4HTM SNP Silent 3 49043565 C G 29 54 HNSC TCGA-CN-5369 P4HTM DEL Frame_Shift_Del 3 49042369 G - 35 60 HNSC TCGA-CV-6952 P4HTM SNP Missense_Mutation 3 49042401 G A 43 96 BRCA TCGA-D8-A1X6 P4HTM SNP Missense_Mutation 3 49044240 T C 62 60 BLCA TCGA-DK-A2I4 P4HTM SNP Missense_Mutation 3 49039971 G A 45 91