ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62505 PHF1 SNP Synonymous 6 33383833 T C 55 54 LUAD LUAD-S01413 PHF1 SNP Missense_Mutation 6 33383630 A G 13 59 MEL ME009 PHF1 SNP Missense_Mutation 6 33382139 G A 43 97 MEL MEL-UKRV-Mel-6 PHF1 SNP Missense_Mutation 6 33383627 C T 22 73 LUAD TCGA-05-4396 PHF1 SNP Missense_Mutation 6 33381849 G T 39 70 LUAD TCGA-05-4396 PHF1 SNP Missense_Mutation 6 33383373 C A 21 55 GBM TCGA-06-5417 PHF1 SNP Silent 6 33382595 A G 11 80 GBM TCGA-08-0386 PHF1 SNP Silent 6 33380059 C T 28 83 LUAD TCGA-17-Z020 PHF1 SNP Nonsense_Mutation 6 33382864 C T 25 56 GBM TCGA-32-1977 PHF1 DEL Frame_Shift_Del 6 33382871 C - 26 73 LUAD TCGA-38-4627 PHF1 SNP Missense_Mutation 6 33380553 G A 48 87 LUSC TCGA-60-2715 PHF1 SNP Missense_Mutation 6 33381294 A G 5 87 OV TCGA-61-1998 PHF1 SNP Synonymous 6 33382068 G A 33 82 CRC TCGA-AG-A014 PHF1 SNP Missense_Mutation 6 33383799 G A 39 89 UCEC TCGA-AP-A051 PHF1 SNP Silent 6 33381302 G A 34 67 UCEC TCGA-AP-A059 PHF1 SNP Silent 6 33382520 G A 33 59 UCEC TCGA-AP-A0LM PHF1 SNP Missense_Mutation 6 33383661 C T 32 68 UCEC TCGA-AP-A0LM PHF1 SNP Missense_Mutation 6 33383820 G T 39 59 UCEC TCGA-AX-A0J1 PHF1 SNP Missense_Mutation 6 33380564 C T 31 64 UCEC TCGA-B5-A0JY PHF1 SNP Missense_Mutation 6 33383412 C T 23 45 KIRC TCGA-BP-5000 PHF1 INS Frame_Shift_Ins 6 33382506 - T 8 66 HNSC TCGA-CQ-5334 PHF1 SNP Missense_Mutation 6 33382536 T A 51 62 UCEC TCGA-D1-A176 PHF1 SNP Silent 6 33381251 A G 8 47 UCEC TCGA-EY-A1GS PHF1 SNP Silent 6 33382810 G A 45 59 BLCA TCGA-G2-A2EO PHF1 SNP Silent 6 33380560 G A 36 59 BLCA TCGA-G2-A2EO PHF1 SNP Missense_Mutation 6 33383647 G C 37 51 BLCA TCGA-G2-A2EO PHF1 SNP Silent 6 33383743 G A 41 54 BLCA TCGA-G2-A2EO PHF1 SNP Missense_Mutation 6 33383754 G C 41 69 BLCA TCGA-GV-A3JZ PHF1 SNP Missense_Mutation 6 33380128 C T 31 79