ID   XPCSH5BA
AC   CVCL_1F29
SY   Xeroderma Pigmentosum/Cockayne Syndrome Heterozygote 5 BAsel; GM13028
DR   CLO; CLO_0014002
DR   BioSample; SAMN00802028
DR   Coriell; GM13028
DR   Wikidata; Q54846271
CC   Sequence variation: Mutation; HGNC; HGNC:3435; ERCC3; Simple; p.Phe99Ser (c.296T>C); ClinVar=VCV000016583; Zygosity=Heterozygous (Coriell=GM13028).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   71Y
CA   Finite cell line
DT   Created: 08-07-15; Last updated: 19-12-24; Version: 13
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