{{Rsnum
|rsid=121908828
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TMEM127
|position=96254106
|Gene_s=TMEM127
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=121908828
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=96919844
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050068000a01000002110100
|GENEINFO=TMEM127:55654
|GENE_NAME=TMEM127
|GENE_ID=55654
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.96919844C>T
|CLNORIGIN=1
|CLNSIG=4
|CLNCUI=171300
|CLNDBN=Pheochromocytoma
|Tags=RV;PM;PMC;NSM;REF;OTHERKG;LSD;OM
|CLNDSDB=OMIM
|CLNDSDBID=171300
|Disease=Pheochromocytoma
}}{{PMID|21156949}} Spectrum and prevalence of FP/TMEM127 gene mutations in pheochromocytomas and paragangliomas.
{{omim
|id=171300
|rsnum=121908828
}}