{{Rsnum
|rsid=387907099
|Chromosome=2
|position=98604134
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=COA5
|Gene_s=COA5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=2
|CLNACC=RCV000024082.1
|CLNALLE=1
|CLNDBN=CARDIOMYOPATHY, HYPERTROPHIC, LETHAL NEONATAL, DUE TO CYTOCHROME c OXIDASE DEFICIENCY
|CLNHGVS=NC_000002.11:g.99220597C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=613920.0001
|Disease=CARDIOMYOPATHY
|FwdALT=C
|FwdREF=G
|REF=C
|RSPOS=99220597
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387907099
|GENEINFO=COA5:493753
|GENE_ID=493753
|GENE_NAME=COA5
}}