{{Rsnum
|rsid=386833612
|Chromosome=10
|position=124405548
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TGGGG)
|geno3=(TGGGG;TGGGG)
|Gene=OAT
|Gene_s=OAT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Orientation=minus
}}{{ClinVar
|ALT=A
|CHROM=10
|CLNACC=RCV000049539.1
|CLNALLE=1
|CLNDBN=Ornithine aminotransferase deficiency
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0599035:258870:414:276426004
|CLNHGVS=NC_000010.10:g.126094117_126094121delCCCCA
|CLNSIG=4
|Disease=Ornithine aminotransferase deficiency
|FwdREF=GGGGT
|REF=ACCCCA
|RSPOS=126094116
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050068000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=386833612
|GENEINFO=OAT:4942
|GENE_ID=4942
|GENE_NAME=OAT
}}{{PMID Auto
|PMID=22674428
|Title=Gyrate atrophy: clinical and genetic findings in a female without arginine-restricted diet during her first 39 years of life and report of a new OAT gene mutation.
}}