ID   IIIC-BCHM
AC   CVCL_4409
DR   Wikidata; Q54897427
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Thr125Thr (c.375G>A); ClinVar=VCV000177825; Zygosity=Heterozygous; Note=Impairs TP53 splicing dramatically (from parent cell line).
CC   Caution: Was briefly displayed in Cell Bank Australia under catalog number CBA-0160 but was never intended to be distributed.
CC   Derived from site: In situ; Breast, stroma; UBERON=UBERON_0003584.
DI   NCIt; C3476; Li-Fraumeni syndrome
DI   ORDO; Orphanet_524; Li-Fraumeni syndrome
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_ZT89 ! IIICF
SX   Female
AG   30-40Y
CA   Undefined cell line type
DT   Created: 04-04-12; Last updated: 29-06-23; Version: 15
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