{{Rsnum
|rsid=121912681
|Chromosome=16
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TTC)
|geno3=(TTC;TTC)
|Gene=APRT
|position=88809722
|Gene_s=APRT,CDT1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=102600
|rsnum=121912681
|variant=0001
}}{{ClinVar
|rsid=121912681
|Reversed=1
|FwdREF=TCT
|FwdALT=
|REF=AGAA
|ALT=A
|RSPOS=88876126
|CHROM=16
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=CDT1:81620; APRT:353
|GENE_NAME=CDT1; APRT
|GENE_ID=81620; 353
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000016.9:g.88876130_88876132delGAA
|CLNORIGIN=1
|CLNSIG=5
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNACC=RCV000019956.27
|CLNDBN=Aprt deficiency
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=102600.0001
|Disease=Aprt deficiency
}}