{{Rsnum
|rsid=121434452
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TUFM
|position=28844008
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MIR4721,TUFM
}}{{omim
|id=602389
|rsnum=121434452
|variant=0001
}}{{ClinVar
|rsid=121434452
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=28855329
|CHROM=16
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=TUFM:7284; MIR4721:100616256
|GENE_NAME=TUFM; MIR4721
|GENE_ID=7284; 100616256
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.28855329C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602389.0001
|CLNSIG=5
|CLNCUI=C1857682
|CLNDBN=Combined oxidative phosphorylation deficiency 4
|Disease=Combined oxidative phosphorylation deficiency 4
|CLNACC=RCV000007698.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857682:610678:254925
}}