ttype patient gene classification type chr pos ref_allele newbase context65 cons46 LUAD LUAD-B00416 TMEM109 SNP Silent 11 60689424 G T 47 69 GBM TCGA-27-1833 TMEM109 SNP Missense_Mutation 11 60687272 G A 40 53 LUAD TCGA-44-2659 TMEM109 INS Frame_Shift_Ins 11 60689518 - C 54 46 LUSC TCGA-46-3769 TMEM109 SNP Nonsense_Mutation 11 60687196 G T 43 50 OV TCGA-61-2109 TMEM109 SNP Missense_Mutation 11 60687238 C T 24 60 GBM TCGA-76-6661 TMEM109 SNP Missense_Mutation 11 60687316 G C 36 54 CRC TCGA-AA-3554 TMEM109 SNP Missense_Mutation 11 60687179 G T 34 58 CRC TCGA-AA-3947 TMEM109 SNP Missense_Mutation 11 60689458 C T 23 67 CRC TCGA-AG-A002 TMEM109 SNP Silent 11 60689289 C T 30 50 UCEC TCGA-AP-A051 TMEM109 SNP Missense_Mutation 11 60687314 C A 21 79 UCEC TCGA-AP-A051 TMEM109 SNP Silent 11 60689493 C T 19 50 UCEC TCGA-B5-A0JY TMEM109 SNP Missense_Mutation 11 60689269 A C 9 54 UCEC TCGA-B5-A11N TMEM109 SNP Missense_Mutation 11 60687365 C A 26 52 KIRC TCGA-BP-4337 TMEM109 SNP Silent 11 60689310 A T 11 42 KIRC TCGA-BP-4758 TMEM109 SNP Missense_Mutation 11 60689459 G A 39 65 HNSC TCGA-CV-6441 TMEM109 SNP Silent 11 60689394 G C 45 60 UCEC TCGA-D1-A103 TMEM109 SNP Silent 11 60687345 T C 55 50 CARC Carc-BWH4 TMEM109 SNP Missense_Mutation 11 60687272 G A 40 53