ID   IIICF/c/rasT21
AC   CVCL_4416
DR   Wikidata; Q54897436
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Thr125Thr (c.375G>A); ClinVar=VCV000177825; Zygosity=Hemizygous; Note=Impairs TP53 splicing dramatically (from parent cell line).
CC   Caution: Was briefly displayed in Cell Bank Australia under catalog number CBA-0040 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_4415 ! IIICF/c
SX   Female
AG   30-40Y
CA   Transformed cell line
DT   Created: 04-04-12; Last updated: 19-12-24; Version: 14
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