{{Rsnum
|rsid=104894560
|Chromosome=17
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=COX10
|position=14102230
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=COX10
}}{{omim
|id=602125
|rsnum=104894560
|variant=0001
}}{{ClinVar
|rsid=104894560
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=14005547
|CHROM=17
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=COX10:1352
|GENE_NAME=COX10
|GENE_ID=1352
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000017.10:g.14005547C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=602125.0001
|CLNSIG=5
|CLNCUI=C0268237
|CLNDBN=Cytochrome-c oxidase deficiency; ENCEPHALOPATHY, PROGRESSIVE MITOCHONDRIAL, WITH PROXIMAL RENAL TUBULOPATHY DUE TO MITOCHONDRIAL COMPLEX IV DEFICIENCY
|Disease=Cytochrome-c oxidase deficiency; ENCEPHALOPATHY
|CLNACC=RCV000007956.2; RCV000007957.1
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:SNOMED_CT
|CLNDSDBID=C0268237:220110:67434000
}}