ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-F00162 MEOX1 SNP Missense_Mutation 17 41738736 G A 40 68 MEL ME037 MEOX1 SNP Missense_Mutation 17 41719307 C T 30 81 MEL MEL-JWCI-WGS-22 MEOX1 SNP Missense_Mutation 17 41738560 C T 30 69 MEL MEL-JWCI-WGS-39 MEOX1 SNP Nonsense_Mutation 17 41738674 C A 30 77 MEL MEL-JWCI-WGS-5 MEOX1 SNP Missense_Mutation 17 41738631 G A 41 65 LUAD TCGA-05-4396 MEOX1 SNP Missense_Mutation 17 41738500 C A 23 54 LUAD TCGA-17-Z001 MEOX1 SNP Missense_Mutation 17 41738663 G T 33 67 LUAD TCGA-44-6774 MEOX1 SNP Nonsense_Mutation 17 41738726 G T 44 70 LUAD TCGA-44-6778 MEOX1 SNP Missense_Mutation 17 41738613 G A 35 67 BRCA TCGA-A8-A09G MEOX1 SNP Missense_Mutation 17 41738538 C T 26 63 CRC TCGA-AA-3684 MEOX1 SNP Missense_Mutation 17 41738541 A G 7 59 UCEC TCGA-AP-A059 MEOX1 SNP Missense_Mutation 17 41720899 C T 27 94 UCEC TCGA-AP-A059 MEOX1 SNP Missense_Mutation 17 41738729 C T 19 35 UCEC TCGA-AP-A0LM MEOX1 SNP Nonsense_Mutation 17 41720948 G A 38 54 UCEC TCGA-AP-A0LM MEOX1 SNP Missense_Mutation 17 41738596 G A 38 63 UCEC TCGA-AX-A05Z MEOX1 SNP Missense_Mutation 17 41738738 C T 31 43 KIRC TCGA-B8-4620 MEOX1 SNP Nonsense_Mutation 17 41738797 G T 44 57 HNSC TCGA-BA-4078 MEOX1 SNP Missense_Mutation 17 41738516 G A 42 59 BLCA TCGA-BT-A2LB MEOX1 SNP Missense_Mutation 17 41719371 C G 29 94 UCEC TCGA-D1-A177 MEOX1 SNP Nonsense_Mutation 17 41738739 G A 38 65 BRCA TCGA-D8-A1Y1 MEOX1 SNP Missense_Mutation 17 41738729 C T 19 35