ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-25 ASCL3 SNP Silent 11 8959406 C T 22 52 LUAD TCGA-05-4382 ASCL3 SNP Missense_Mutation 11 8959435 G T 42 88 LUAD TCGA-05-4402 ASCL3 SNP Missense_Mutation 11 8959371 T G 57 93 LUAD TCGA-05-4420 ASCL3 SNP Silent 11 8959544 C A 26 53 LUAD TCGA-17-Z050 ASCL3 SNP Missense_Mutation 11 8959359 C T 27 100 LUAD TCGA-50-5939 ASCL3 SNP Nonsense_Mutation 11 8959615 C A 30 73 LUSC TCGA-66-2734 ASCL3 SNP Nonsense_Mutation 11 8959439 G T 40 41 BRCA TCGA-A1-A0SJ ASCL3 SNP Missense_Mutation 11 8959533 G C 43 67 CRC TCGA-AA-3977 ASCL3 SNP Missense_Mutation 11 8959296 G A 38 100 AML TCGA-AB-2808 ASCL3 SNP Silent 11 8959691 G A 46 53 CRC TCGA-AG-A002 ASCL3 SNP Missense_Mutation 11 8959396 G A 38 52 UCEC TCGA-AP-A051 ASCL3 SNP Missense_Mutation 11 8959343 C A 24 54 UCEC TCGA-AP-A059 ASCL3 SNP Silent 11 8959454 C T 18 48 KIRC TCGA-BP-4176 ASCL3 SNP Nonsense_Mutation 11 8959460 G T 48 74 UCEC TCGA-BS-A0UF ASCL3 SNP Missense_Mutation 11 8959238 C A 32 58 HNSC TCGA-CR-7392 ASCL3 SNP Missense_Mutation 11 8959494 C T 25 60 BRCA TCGA-E2-A14S ASCL3 SNP Silent 11 8959451 G A 38 49 BRCA TCGA-E9-A1R2 ASCL3 DEL Frame_Shift_Del 11 8959263 AGAAG - 7 91