{{Rsnum
|rsid=281860264
|Chromosome=16
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=APRT
|position=88810451
|Gene_s=APRT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=16
|CLNACC=RCV000033905.2
|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.88876859C>T
|CLNSIG=5
|CLNSRC=GeneReviews
|CLNSRCID=NBK100238
|Disease=Deficiency of AMP pyrophorylase
|FwdALT=A
|FwdREF=G
|REF=C
|RSPOS=88876859
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;SLO;NSN;REF;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050360000601000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=281860264
}}