{{Rsnum
|rsid=281860266
|Chromosome=16
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=APRT
|position=88809793
|Gene_s=APRT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=16
|CLNACC=RCV000033909.2
|CLNALLE=1
|CLNDBN=Deficiency of AMP pyrophorylase
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK100238:C0268120:614723:976:124274002
|CLNHGVS=NC_000016.9:g.88876201C>A
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK100238
|Disease=Deficiency of AMP pyrophorylase
|FwdALT=T
|FwdREF=G
|REF=C
|RSPOS=88876201
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD
|VC=SNV
|VP=0x050360000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=281860266
|GENEINFO=APRT:353
|GENE_ID=353
|GENE_NAME=APRT
}}