ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-105 ZNF660 SNP Silent 3 44636084 T C 56 14 LUAD LUAD-S01467 ZNF660 SNP Missense_Mutation 3 44635851 G T 47 95 MEL MEL-13531 ZNF660 SNP Missense_Mutation 3 44636062 G A 41 65 LUAD TCGA-05-4396 ZNF660 SNP Missense_Mutation 3 44636202 C A 23 59 LUAD TCGA-05-4420 ZNF660 SNP Missense_Mutation 3 44636480 G C 33 60 LUAD TCGA-17-Z056 ZNF660 SNP Missense_Mutation 3 44636579 G C 35 47 LUAD TCGA-49-6745 ZNF660 SNP Missense_Mutation 3 44635871 T A 59 49 CRC TCGA-AA-3555 ZNF660 SNP Missense_Mutation 3 44636398 G T 33 60 CRC TCGA-AG-A002 ZNF660 SNP Silent 3 44636561 C T 20 56 UCEC TCGA-AP-A051 ZNF660 SNP Nonsense_Mutation 3 44636229 C T 27 54 UCEC TCGA-AP-A056 ZNF660 SNP Missense_Mutation 3 44636314 G T 33 72 UCEC TCGA-AP-A0LM ZNF660 SNP Silent 3 44635904 G A 39 45 UCEC TCGA-AP-A0LM ZNF660 SNP Missense_Mutation 3 44636407 G A 40 59 BRCA TCGA-AR-A1AK ZNF660 SNP Nonsense_Mutation 3 44636310 C T 29 55 UCEC TCGA-AX-A05Z ZNF660 SNP Missense_Mutation 3 44636461 G A 37 52 UCEC TCGA-B5-A0JY ZNF660 SNP Missense_Mutation 3 44636382 C A 32 76 UCEC TCGA-B5-A11N ZNF660 SNP Missense_Mutation 3 44636461 G A 37 52 HNSC TCGA-BA-6869 ZNF660 SNP Missense_Mutation 3 44636619 C T 31 54 HNSC TCGA-CN-4728 ZNF660 SNP Silent 3 44635868 G A 33 55 HNSC TCGA-CN-6010 ZNF660 SNP Missense_Mutation 3 44636533 T A 62 86 UCEC TCGA-D1-A17Q ZNF660 SNP Missense_Mutation 3 44635894 G A 37 69 BLCA TCGA-DK-A3IQ ZNF660 SNP Missense_Mutation 3 44636265 G C 41 59