ttype patient gene classification type chr pos ref_allele newbase context65 cons46 BRCA BR-0043 ZSCAN21 SNP Missense_Mutation 7 99655492 C A 29 63 ESO ESO-0125 ZSCAN21 SNP Missense_Mutation 7 99662178 T C 55 55 LUAD LUAD-YINHD ZSCAN21 SNP Silent 7 99654827 C T 30 58 MEL ME049 ZSCAN21 SNP Silent 7 99654713 C T 31 29 MEL MEL-JWCI-WGS-1 ZSCAN21 SNP Missense_Mutation 7 99655370 C T 30 73 MEL MEL-Ma-Mel-114 ZSCAN21 SNP Nonsense_Mutation 7 99661869 C T 29 74 LUAD TCGA-05-4396 ZSCAN21 SNP Missense_Mutation 7 99654658 C A 21 77 LUAD TCGA-05-4396 ZSCAN21 SNP Missense_Mutation 7 99655394 C A 23 41 LUAD TCGA-05-4396 ZSCAN21 SNP Missense_Mutation 7 99661842 G T 47 63 OV TCGA-13-0887 ZSCAN21 SNP Splice_site 7 99661412 T A 52 77 OV TCGA-13-1509 ZSCAN21 SNP Missense_Mutation 7 99661781 C G 22 56 LUSC TCGA-37-5819 ZSCAN21 SNP Missense_Mutation 7 99654654 G T 42 58 LUSC TCGA-60-2720 ZSCAN21 SNP Missense_Mutation 7 99661526 C G 28 51 OV TCGA-61-2092 ZSCAN21 SNP Missense_Mutation 7 99655002 C T 27 55 LUAD TCGA-67-3771 ZSCAN21 SNP Missense_Mutation 7 99662084 G A 41 53 LUAD TCGA-91-6836 ZSCAN21 SNP Missense_Mutation 7 99654933 C A 21 83 BRCA TCGA-A2-A0YJ ZSCAN21 SNP Missense_Mutation 7 99654891 C G 20 69 KIRC TCGA-A3-3385 ZSCAN21 DEL Frame_Shift_Del 7 99661552 A - 9 50 UCEC TCGA-A5-A0GA ZSCAN21 SNP Missense_Mutation 7 99661969 G T 43 92 UCEC TCGA-A5-A0GW ZSCAN21 SNP Missense_Mutation 7 99661471 A T 11 53 AML TCGA-AB-2858 ZSCAN21 SNP Silent 7 99654638 C T 21 58 CRC TCGA-AG-A002 ZSCAN21 SNP Missense_Mutation 7 99661644 C T 19 59 CRC TCGA-AG-A02N ZSCAN21 SNP Missense_Mutation 7 99661734 G A 40 53 UCEC TCGA-AX-A063 ZSCAN21 SNP Missense_Mutation 7 99654858 G A 37 83 KIRC TCGA-B0-5109 ZSCAN21 SNP Missense_Mutation 7 99662005 G A 34 58 UCEC TCGA-BG-A0M2 ZSCAN21 DEL Frame_Shift_Del 7 99661636 GA - 41 77 BRCA TCGA-BH-A0EB ZSCAN21 SNP Missense_Mutation 7 99654841 G A 48 79 HNSC TCGA-CR-7398 ZSCAN21 SNP Missense_Mutation 7 99654694 G A 43 64 HNSC TCGA-CV-6955 ZSCAN21 SNP Missense_Mutation 7 99654858 G A 37 83 BLCA TCGA-DK-A2I4 ZSCAN21 SNP Missense_Mutation 7 99654714 G A 37 54 CARC Carc-Thirlwell7 ZSCAN21 SNP Missense_Mutation 7 99662143 A C 3 66