ttype patient gene classification type chr pos ref_allele newbase context65 cons46 ESO ESO-0149 TMEM213 SNP Missense_Mutation 7 138482910 C T 24 50 MEL MEL-UKRV-Mel-20 TMEM213 SNP Silent 7 138482861 C T 30 57 MEL MEL-UKRV-Mel-6 TMEM213 SNP Nonsense_Mutation 7 138487706 G A 41 81 LUAD TCGA-17-Z026 TMEM213 SNP Splice_site 7 138522652 C T 29 91 LUSC TCGA-33-4583 TMEM213 SNP Silent 7 138487700 C T 19 35 BRCA TCGA-A2-A0SU TMEM213 DEL Frame_Shift_Del 7 138482852 GCAGCGCCTCCCC - 46 53 CRC TCGA-AA-3710 TMEM213 SNP Missense_Mutation 7 138522671 C T 19 70 UCEC TCGA-AX-A05Z TMEM213 SNP Missense_Mutation 7 138487655 C A 32 82 UCEC TCGA-BG-A187 TMEM213 SNP Silent 7 138487709 C A 31 51 KIRC TCGA-BP-4964 TMEM213 SNP Missense_Mutation 7 138487680 C T 23 57 HNSC TCGA-CV-7440 TMEM213 SNP Missense_Mutation 7 138487681 G A 38 46 UCEC TCGA-D1-A168 TMEM213 SNP Missense_Mutation 7 138486104 G A 38 40 UCEC TCGA-FI-A2F8 TMEM213 SNP Missense_Mutation 7 138487764 G A 41 63 BLCA TCGA-G2-A2EL TMEM213 SNP Nonsense_Mutation 7 138487791 G T 45 81