ttype patient gene classification type chr pos ref_allele newbase context65 cons46 MEL MEL-JWCI-WGS-12 TMEM184C SNP Missense_Mutation 4 148546052 C T 18 80 GBM TCGA-06-1806 TMEM184C SNP Silent 4 148545074 A G 15 54 LUAD TCGA-17-Z026 TMEM184C SNP Missense_Mutation 4 148555046 C T 29 100 LUSC TCGA-60-2715 TMEM184C SNP Missense_Mutation 4 148549579 G A 40 54 CRC TCGA-AA-3850 TMEM184C SNP Silent 4 148554111 G A 40 33 CRC TCGA-AA-3977 TMEM184C SNP Missense_Mutation 4 148554110 C T 19 100 CRC TCGA-AA-A01I TMEM184C SNP Missense_Mutation 4 148554145 G A 39 100 CRC TCGA-AG-A002 TMEM184C SNP Missense_Mutation 4 148545976 G A 39 64 KIRC TCGA-AK-3444 TMEM184C SNP Missense_Mutation 4 148555434 C T 32 98 UCEC TCGA-AP-A056 TMEM184C SNP Missense_Mutation 4 148545105 C A 18 100 UCEC TCGA-AP-A059 TMEM184C SNP Missense_Mutation 4 148555323 G A 39 97 UCEC TCGA-AP-A0LM TMEM184C SNP Missense_Mutation 4 148544995 A G 6 92 UCEC TCGA-AX-A0J0 TMEM184C SNP Missense_Mutation 4 148545217 C A 32 74 KIRC TCGA-B0-5095 TMEM184C SNP Missense_Mutation 4 148545244 G A 33 100 KIRC TCGA-B2-4099 TMEM184C SNP Splice_site 4 148545115 G C 35 100 KIRC TCGA-BP-5173 TMEM184C SNP Missense_Mutation 4 148555356 T G 64 90 HNSC TCGA-CN-4728 TMEM184C SNP Missense_Mutation 4 148539207 G A 40 56 HNSC TCGA-CN-6994 TMEM184C SNP Missense_Mutation 4 148545966 G C 45 63 UCEC TCGA-D1-A103 TMEM184C SNP Missense_Mutation 4 148552559 C T 32 87 HNSC TCGA-H7-7774 TMEM184C SNP Missense_Mutation 4 148554974 C T 29 100