{{Rsnum
|rsid=387906584
|Chromosome=16
|Orientation=minus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=APRT
|position=88809699
|Gene_s=APRT,CDT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=16
|CLNACC=RCV000019964.26
|CLNALLE=1
|CLNDBN=Aprt deficiency
|CLNHGVS=NC_000016.9:g.88876107C>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=102600.0009
|Disease=Aprt deficiency
|FwdALT=C
|FwdREF=G
|REF=C
|RSPOS=88876107
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD
|VC=SNV
|VP=0x050060000000000002100100
|WGT=0
|dbSNPBuildID=137
|rsid=387906584
|GENEINFO=CDT1:81620; APRT:353
|GENE_ID=81620; 353
|GENE_NAME=CDT1; APRT
}}