ID   AG24467
AC   CVCL_UY16
DR   Coriell; AG24467
DR   Wikidata; Q93323309
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; HGNC:12791; WRN; Simple; p.Asn1197Thrfs*2 (c.3590delA); ClinVar=VCV000038890; Zygosity=Homozygous (Coriell=AG24467).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C3447; Werner syndrome
DI   ORDO; Orphanet_902; Werner syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   39Y
CA   Finite cell line
DT   Created: 25-02-19; Last updated: 19-12-24; Version: 10
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