{{Rsnum
|rsid=199476124
|Chromosome=MT
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ANKRD20A19P
|position=3949
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MT-CO1
}}{{ClinVar
|ALT=C
|CHROM=MT
|CLNACC=RCV000010388.1
|CLNALLE=1
|CLNDBN=Juvenile myopathy, encephalopathy, lactic acidosis AND stroke
|CLNDSDB=GeneReviews:GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1224:NBK1233:C0162671:540000:550:39925003
|CLNHGVS=NC_012920.1:m.3949T>C
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=516000.0014
|Disease=Juvenile myopathy
|FwdALT=C
|FwdREF=T
|REF=T
|RSPOS=3949
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=199476124
}}