{{Rsnum
|rsid=386834131
|Chromosome=8
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=CLN8
|position=1771561
|Gene_s=CLN8
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=8
|CLNACC=RCV000050124.1
|CLNALLE=1
|CLNDBN=Ceroid lipofuscinosis neuronal 8
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet:Orphanet
|CLNDSDBID=NBK1428:C1838570:600143:168491:228354:79264
|CLNHGVS=NC_000008.10:g.1719727C>T
|CLNSIG=4
|Disease=Ceroid lipofuscinosis neuronal 8
|FwdALT=T
|FwdREF=C
|REF=C
|RSPOS=1719727
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;PMC;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050068000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=386834131
|GENEINFO=CLN8:2055
|GENE_ID=2055
|GENE_NAME=CLN8
}}{{PMID Auto
|PMID=21990111
|Title=Update of the mutation spectrum and clinical correlations of over 360 mutations in eight genes that underlie the neuronal ceroid lipofuscinoses.
}}