{{Rsnum
|rsid=67486158
|Chromosome=X
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OTC
|position=38367361
|Gene_s=OTC
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|rsid=67486158
|Reversed=0
|FwdREF=G
|FwdALT=A,T
|REF=G
|ALT=A,T
|RSPOS=38226614
|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.38226614G>A; NC_000023.10:g.38226614G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=0
|CLNSRCID=300461.0017
|CLNSIG=5
|CLNCUI=C0268542
|CLNDBN=not provided; Ornithine carbamoyltransferase deficiency
|Disease=not provided; Ornithine carbamoyltransferase deficiency
|CLNACC=RCV000083345.1; RCV000011749.8; RCV000083346.1
|Tags=PM;PMC;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK154378:C0268542:311250:664:80908008
}}

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

{{PMID Auto
|PMID=1353535
|Title=Site specific screening for point mutations in ornithine transcarbamylase deficiency.
|OA=1
}}

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