{{Rsnum
|rsid=201431517
|Chromosome=15
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MTFMT
|position=65021533
|Gene_s=MTFMT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=15
|CLNACC=RCV000033047.2; RCV000033048.2
|CLNALLE=1
|CLNDBN=Combined oxidative phosphorylation deficiency 15; Leigh syndrome due to mitochondrial complex I deficiency
|CLNDSDB=MedGen:OMIM; MedGen
|CLNDSDBID=CN162965:614947; C1838951
|CLNHGVS=NC_000015.9:g.65313871G>A
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=611766.0001
|Disease=Combined oxidative phosphorylation deficiency 15; Leigh syndrome due to mitochondrial complex I deficiency
|FwdALT=A
|FwdREF=G
|GENEINFO=MTFMT:123263
|GENE_ID=123263
|GENE_NAME=MTFMT
|REF=G
|RSPOS=65313871
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;S3D;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050260000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=201431517
}}