ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0459 PCGF5 SNP Nonsense_Mutation 10 93008311 C T 19 66 MEL MEL-JWCI-WGS-21 PCGF5 SNP Missense_Mutation 10 93008281 G A 41 100 LUAD TCGA-05-4396 PCGF5 SNP Missense_Mutation 10 93000289 C A 21 100 LUAD TCGA-05-4410 PCGF5 SNP Missense_Mutation 10 93011157 G A 48 98 GBM TCGA-14-2554 PCGF5 SNP Silent 10 93038067 C T 31 44 GBM TCGA-32-2498 PCGF5 SNP Missense_Mutation 10 93031452 C A 29 75 LUSC TCGA-34-5231 PCGF5 SNP Missense_Mutation 10 93008287 A G 16 91 LUAD TCGA-44-6778 PCGF5 SNP Missense_Mutation 10 93000258 G T 48 100 KIRC TCGA-A3-3320 PCGF5 DEL Frame_Shift_Del 10 93011143 TA - 53 50 UCEC TCGA-A5-A0GB PCGF5 SNP Missense_Mutation 10 92982636 C T 18 98 CRC TCGA-AA-3672 PCGF5 SNP Missense_Mutation 10 93011160 T C 61 89 CRC TCGA-AG-A002 PCGF5 DEL Frame_Shift_Del 10 93021137 A - 13 90 UCEC TCGA-AP-A056 PCGF5 SNP Nonsense_Mutation 10 93021104 C T 31 84 UCEC TCGA-AP-A059 PCGF5 SNP Silent 10 93024196 G A 46 54 UCEC TCGA-AP-A0LT PCGF5 SNP Silent 10 93008435 T C 59 51 UCEC TCGA-AX-A05Z PCGF5 SNP Silent 10 93038067 C T 31 44 UCEC TCGA-B5-A0JY PCGF5 SNP Missense_Mutation 10 93038067 C A 31 44 UCEC TCGA-B5-A11E PCGF5 SNP Missense_Mutation 10 93008299 G A 44 86 UCEC TCGA-B5-A11E PCGF5 SNP Missense_Mutation 10 93031398 C T 31 75 HNSC TCGA-BA-7269 PCGF5 SNP Nonsense_Mutation 10 93038049 T G 50 63 UCEC TCGA-BG-A0VZ PCGF5 SNP Missense_Mutation 10 92982723 C T 19 85 UCEC TCGA-BS-A0TC PCGF5 SNP Nonsense_Mutation 10 93021104 C T 31 84 UCEC TCGA-BS-A0UL PCGF5 SNP Silent 10 93000278 C T 25 61 HNSC TCGA-CR-7398 PCGF5 SNP Missense_Mutation 10 93011162 C G 19 84 BRCA TCGA-E2-A15R PCGF5 SNP Missense_Mutation 10 93021117 G A 40 98