ttype patient gene classification type chr pos ref_allele newbase context65 cons46 HNSC HN_62298 TMEM184A SNP Missense 7 1588314 C T 23 99 HNSC HN_62318 TMEM184A SNP Splice_site 7 1589943 G A 45 51 HNSC HN_62318 TMEM184A SNP Synonymous 7 1590553 G A 45 85 LUAD LUAD-B00915 TMEM184A SNP Missense_Mutation 7 1586776 C G 30 100 LUAD LUAD-CHTN-MAD04-00674 TMEM184A SNP Missense_Mutation 7 1588284 C T 27 47 LUAD LUAD-S01381 TMEM184A SNP Missense_Mutation 7 1590566 A G 12 91 LUAD LUAD-YINHD TMEM184A SNP Missense_Mutation 7 1586811 G T 39 56 MEL ME016 TMEM184A SNP Silent 7 1586645 C T 30 47 MEL MEL-JWCI-WGS-25 TMEM184A SNP Silent 7 1594914 G A 45 55 MEL MEL-Ma-Mel-102 TMEM184A SNP Silent 7 1586603 G A 35 51 MEL MEL-Ma-Mel-102 TMEM184A SNP Silent 7 1595067 C T 31 28 MEL MEL-Ma-Mel-54a TMEM184A SNP Missense_Mutation 7 1587422 G A 42 100 MEL MEL-Ma-Mel-63 TMEM184A SNP Silent 7 1589786 G A 47 57 MEL MEL-Ma-Mel-85 TMEM184A SNP Silent 7 1595103 C T 30 53 MEL MEL-Ma-Mel-94 TMEM184A SNP Silent 7 1588195 G A 41 64 LUAD TCGA-05-4396 TMEM184A SNP Silent 7 1594944 C A 23 42 LUAD TCGA-05-4410 TMEM184A SNP Silent 7 1589783 G T 37 41 GBM TCGA-06-0171 TMEM184A SNP Silent 7 1588261 G A 40 54 LUSC TCGA-22-4599 TMEM184A SNP Missense_Mutation 7 1589575 G C 33 98 LUSC TCGA-39-5036 TMEM184A SNP Missense_Mutation 7 1587401 G C 46 69 LUAD TCGA-44-2655 TMEM184A SNP Silent 7 1590517 G A 42 86 LUAD TCGA-49-6743 TMEM184A SNP Missense_Mutation 7 1586636 C G 32 82 CRC TCGA-AA-3864 TMEM184A SNP Silent 7 1589819 G A 40 48 UCEC TCGA-AP-A059 TMEM184A SNP Silent 7 1590606 G A 35 77 UCEC TCGA-AP-A059 TMEM184A SNP Splice_Site 7 1594901 C T 18 93 UCEC TCGA-AP-A0LM TMEM184A SNP Missense_Mutation 7 1590531 C T 31 86 BLCA TCGA-BT-A20V TMEM184A SNP Nonsense_Mutation 7 1594929 C T 30 79 BLCA TCGA-BT-A2LA TMEM184A SNP Missense_Mutation 7 1588230 C T 30 100 HNSC TCGA-CV-5434 TMEM184A SNP Nonsense_Mutation 7 1590490 G T 36 75 UCEC TCGA-DI-A0WH TMEM184A SNP Missense_Mutation 7 1588260 C T 27 99 HNSC TCGA-DQ-7590 TMEM184A SNP Silent 7 1588285 G A 40 66 HNSC TCGA-HD-7754 TMEM184A SNP Missense_Mutation 7 1595084 C T 19 51