{{Rsnum
|rsid=121434325
|Chromosome=5
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ERCC8
|position=60904794
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ERCC8
}}{{omim
|id=609412
|rsnum=121434325
|variant=0004
}}{{ClinVar
|rsid=121434325
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=60200621
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=ERCC8:1161
|GENE_NAME=ERCC8
|GENE_ID=1161
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.60200621G>A
|CLNSRC=OMIM Allelic Variant; UniProtKB (variants)
|CLNORIGIN=1
|CLNSRCID=609412.0004; VAR_025380
|CLNSIG=5
|CLNCUI=C0751039
|CLNDBN=Cockayne syndrome type A; not provided
|Disease=Cockayne syndrome type A; not provided
|CLNACC=RCV000001787.2; RCV000059647.1
|Tags=RV;PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1342:C0751039:216400:191:21086008
}}{{PMID Auto
|PMID=15744458
|Title=Characterisation of novel mutations in Cockayne syndrome type A and xeroderma pigmentosum group C subjects.
}}