ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-S41 PTX3 SNP Missense_Mutation 3 157160687 G T 36 48 LUAD TCGA-05-4396 PTX3 SNP Nonsense_Mutation 3 157160202 G T 47 74 LUSC TCGA-43-2578 PTX3 SNP Missense_Mutation 3 157160709 A T 16 53 LUAD TCGA-49-4486 PTX3 SNP Missense_Mutation 3 157160340 C G 32 84 LUSC TCGA-60-2722 PTX3 SNP Missense_Mutation 3 157160481 G C 47 65 CRC TCGA-AA-3543 PTX3 SNP Missense_Mutation 3 157160572 G T 46 86 CRC TCGA-AA-3544 PTX3 SNP Missense_Mutation 3 157160185 G A 40 97 UCEC TCGA-AP-A056 PTX3 SNP Silent 3 157154737 G A 37 52 UCEC TCGA-AP-A059 PTX3 SNP Missense_Mutation 3 157154762 G A 46 53 HNSC TCGA-BA-5556 PTX3 SNP Missense_Mutation 3 157160520 C T 29 76 BRCA TCGA-BH-A1EV PTX3 SNP Missense_Mutation 3 157160269 C T 17 97 HNSC TCGA-CR-6484 PTX3 SNP Silent 3 157160249 C T 24 59 HNSC TCGA-CV-7414 PTX3 SNP Missense_Mutation 3 157160376 G C 33 81 UCEC TCGA-D1-A17D PTX3 SNP Missense_Mutation 3 157160184 C T 27 82 BLCA TCGA-DK-A3IU PTX3 SNP Missense_Mutation 3 157160451 G A 33 54