ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62505 SLC39A4 SNP Missense 8 145639365 G T 33 65 LUAD LUAD-RT-S01721 SLC39A4 SNP Missense_Mutation 8 145638162 T C 57 83 LUAD LUAD-S01478 SLC39A4 SNP Silent 8 145642087 C A 29 50 MEL ME032 SLC39A4 SNP Missense_Mutation 8 145641343 C T 22 51 MM MM-0581 SLC39A4 SNP Missense_Mutation 8 145640363 C T 30 65 MM MM-0639 SLC39A4 SNP Silent 8 145641254 C T 23 48 PRAD PR-02-1899 SLC39A4 SNP Silent 8 145637976 G A 38 52 LUAD TCGA-05-4418 SLC39A4 DEL In_Frame_Del 8 145637952 CAG - 17 53 OV TCGA-13-1510 SLC39A4 SNP Silent 8 145638009 G A 41 48 LUSC TCGA-18-3419 SLC39A4 SNP Silent 8 145638176 G A 39 32 LUSC TCGA-21-1070 SLC39A4 SNP Missense_Mutation 8 145640760 G T 38 54 GBM TCGA-27-2523 SLC39A4 SNP Missense_Mutation 8 145642115 G A 38 22 LUSC TCGA-34-5928 SLC39A4 SNP Missense_Mutation 8 145641346 C T 31 65 LUAD TCGA-64-1680 SLC39A4 SNP Silent 8 145640272 C T 29 59 LUAD TCGA-91-6831 SLC39A4 SNP Missense_Mutation 8 145642092 G T 33 64 CRC TCGA-AG-A002 SLC39A4 SNP Splice_site 8 145640359 G A 40 58 UCEC TCGA-AJ-A23M SLC39A4 SNP Nonsense_Mutation 8 145638918 C A 29 57 UCEC TCGA-AP-A059 SLC39A4 SNP Silent 8 145638149 G A 38 43 UCEC TCGA-AX-A0J0 SLC39A4 SNP Missense_Mutation 8 145639378 C A 32 53 BRCA TCGA-BH-A208 SLC39A4 SNP Silent 8 145638248 G A 37 63 KIRC TCGA-BP-4165 SLC39A4 SNP Splice_Site 8 145638895 A C 6 54 HNSC TCGA-CR-7365 SLC39A4 SNP Missense_Mutation 8 145638738 C T 31 80 HNSC TCGA-CV-5441 SLC39A4 SNP Silent 8 145642057 C A 21 82 HNSC TCGA-CV-6936 SLC39A4 SNP Missense_Mutation 8 145640760 G T 38 54 KIRC TCGA-CW-5589 SLC39A4 SNP Missense_Mutation 8 145642062 C T 27 51 UCEC TCGA-D1-A16F SLC39A4 SNP Missense_Mutation 8 145638016 G A 43 92 UCEC TCGA-D1-A17A SLC39A4 SNP Missense_Mutation 8 145640383 C T 28 54 BRCA TCGA-E9-A22A SLC39A4 SNP Missense_Mutation 8 145640174 T A 55 56