{{Rsnum
|rsid=281860265
|Chromosome=16
|Orientation=minus
|geno1=(-;-)
|geno2=(-;CCGA)
|geno3=(CCGA;CCGA)
|Gene=APRT
|position=88810482
|Gene_s=APRT
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=TTCGG
|CHROM=16
|CLNACC=RCV000019961.25; RCV000033904.2
|CLNALLE=1
|CLNDBN=Aprt deficiency; Deficiency of AMP pyrophorylase
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK100238:C0268120:614723:976:124274002
|CLNHGVS=NC_000016.9:g.88876891_88876894dupTCGG
|CLNSIG=5
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNSRCID=NBK100238; 102600.0006
|Disease=Aprt deficiency; Deficiency of AMP pyrophorylase
|FwdALT=CCGA
|REF=T
|RSPOS=88876890
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;S3D;SLO;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050360000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=281860265
|GENEINFO=APRT:353
|GENE_ID=353
|GENE_NAME=APRT
}}