{{Rsnum
|rsid=143747297
|Chromosome=6
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MTO1
|position=73482061
|Gene_s=MTO1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=6
|CLNACC=RCV000029168.3
|CLNALLE=1
|CLNDBN=Combined oxidative phosphorylation deficiency 10
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=CN130361:614702:314637
|CLNHGVS=NC_000006.11:g.74191784G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=614667.0002
|Disease=Combined oxidative phosphorylation deficiency 10
|FwdALT=A
|FwdREF=G
|GENEINFO=MTO1:25821
|GENE_ID=25821
|GENE_NAME=MTO1
|REF=G
|RSPOS=74191784
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=134
|rsid=143747297
}}