{{Rsnum
|rsid=386833595
|Chromosome=10
|position=124400881
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=OAT
|Gene_s=OAT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=10
|CLNACC=RCV000049521.1
|CLNALLE=1
|CLNDBN=Ornithine aminotransferase deficiency
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0599035:258870:414:276426004
|CLNHGVS=NC_000010.10:g.126089450C>T
|CLNSIG=4
|Disease=Ornithine aminotransferase deficiency
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=126089450
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386833595
|GENEINFO=OAT:4942
|GENE_ID=4942
|GENE_NAME=OAT
}}{{PMID Auto
|PMID=1609808
|Title=Nonsense-codon mutations of the ornithine aminotransferase gene with decreased levels of mutant mRNA in gyrate atrophy.
|OA=1
}}