{{Rsnum
|rsid=387906421
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=TIFAB
|position=14674
|Assembly=GRCh37.p10
|GenomeBuild=37.5
|dbSNPBuild=138
}}{{ClinVar
|ALT=C,G
|CHROM=MT
|CLNACC=RCV000010243.3; RCV000022898.1
|CLNALLE=1; 2
|CLNDBN=Mitochondrial myopathy, infantile, due to reversible cytochrome c oxidase deficiency
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C3151898:500009:254864
|CLNHGVS=NC_012920.1:m.14674T>C; NC_012920.1:m.14674T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=590025.0002; 590025.0003
|Disease=Mitochondrial myopathy
|FwdALT=C,G
|FwdREF=T
|REF=T
|RSPOS=14674
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906421
}}