ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-22 NKX3-1 SNP Missense_Mutation 8 23538973 G A 47 68 MEL MEL-Ma-Mel-65 NKX3-1 SNP Silent 8 23538842 G A 43 47 MEL MEL-Ma-Mel-67 NKX3-1 SNP Missense_Mutation 8 23538750 C T 28 52 LUAD TCGA-05-4396 NKX3-1 SNP Silent 8 23538820 G T 39 49 LUAD TCGA-17-Z042 NKX3-1 SNP Silent 8 23538980 T C 60 51 GBM TCGA-32-1991 NKX3-1 SNP Silent 8 23538761 C T 21 63 LUAD TCGA-71-6725 NKX3-1 SNP Missense_Mutation 8 23538978 C A 23 99 CRC TCGA-AA-A01R NKX3-1 SNP Nonsense_Mutation 8 23539069 G A 46 81 CRC TCGA-AA-A022 NKX3-1 SNP Missense_Mutation 8 23538820 G A 39 49 CRC TCGA-AA-A02O NKX3-1 SNP Missense_Mutation 8 23538913 G A 40 70 UCEC TCGA-AX-A0J0 NKX3-1 SNP Missense_Mutation 8 23539056 C T 31 99 UCEC TCGA-B5-A11E NKX3-1 SNP Missense_Mutation 8 23538795 T C 60 50 BRCA TCGA-BH-A0BZ NKX3-1 SNP Missense_Mutation 8 23538848 C G 25 63 HNSC TCGA-CV-7427 NKX3-1 SNP Silent 8 23538827 G C 35 56