{{Rsnum
|rsid=68026851
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OTC
|position=38401310
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OTC
}}{{omim
|id=300461
|rsnum=68026851
|variant=0002
}}

{{ClinVar
|rsid=68026851
|Reversed=0
|FwdREF=G
|FwdALT=A,C
|REF=G
|ALT=A,C
|RSPOS=38260563
|CHROM=X
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050268000000000002110100
|GENEINFO=OTC:5009
|GENE_NAME=OTC
|GENE_ID=5009
|WGT=0
|VC=SNV
|CLNALLE=1; 2
|CLNHGVS=NC_000023.10:g.38260563G>A; NC_000023.10:g.38260563G>C
|CLNORIGIN=1; 0
|CLNSIG=5
|CLNCUI=
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNACC=RCV000011734.4; RCV000083434.1; RCV000083435.1
|CLNDBN=Ornithine carbamoyltransferase deficiency; not provided
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK154378:C0268542:311250:664:80908008
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=300461.0002
|Disease=Ornithine carbamoyltransferase deficiency; not provided
}}

{{PMID Auto
|PMID=3170748
|Title=Characterization of point mutations in the same arginine codon in three unrelated patients with ornithine transcarbamylase deficiency.
|OA=1
}}

{{PMID Auto
|PMID=9266388
|Title=Identification of 'private' mutations in patients with ornithine transcarbamylase deficiency.
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}