ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-MEX-045 ASPSCR1 SNP Missense_Mutation 17 79952725 A G 6 60 HNSC HN_62505 ASPSCR1 SNP Missense 17 79943422 C G 25 81 MEL ME011 ASPSCR1 SNP Missense_Mutation 17 79970113 C T 18 65 MEL MEL-JWCI-WGS-13 ASPSCR1 SNP Missense_Mutation 17 79941531 G A 43 67 GBM TCGA-06-0155 ASPSCR1 SNP Missense_Mutation 17 79953896 C T 19 62 LUSC TCGA-39-5039 ASPSCR1 SNP Missense_Mutation 17 79974718 C T 21 80 LUAD TCGA-50-5946 ASPSCR1 SNP Missense_Mutation 17 79954395 G T 47 62 LUSC TCGA-66-2793 ASPSCR1 SNP Silent 17 79974979 G A 45 57 CRC TCGA-AA-3845 ASPSCR1 SNP Silent 17 79952744 C T 19 62 CRC TCGA-AA-3949 ASPSCR1 SNP Missense_Mutation 17 79943408 A G 12 76 KIRC TCGA-B0-5706 ASPSCR1 SNP Silent 17 79941541 C T 17 52 UCEC TCGA-B5-A0JY ASPSCR1 SNP Missense_Mutation 17 79943386 C T 31 81 HNSC TCGA-BA-5153 ASPSCR1 SNP Missense_Mutation 17 79954516 G C 48 56 HNSC TCGA-BB-4228 ASPSCR1 SNP Missense_Mutation 17 79966949 G T 44 62 KIRC TCGA-BP-4963 ASPSCR1 SNP Missense_Mutation 17 79954308 G T 36 61 UCEC TCGA-BS-A0TJ ASPSCR1 SNP Missense_Mutation 17 79954420 G A 37 62 BLCA TCGA-BT-A2LB ASPSCR1 SNP Missense_Mutation 17 79954451 C T 29 57 HNSC TCGA-CR-6472 ASPSCR1 SNP Silent 17 79954344 G C 47 44 UCEC TCGA-D1-A103 ASPSCR1 SNP Silent 17 79954311 C T 28 48