ID   S/RG
AC   CVCL_8756
SY   RG
DR   cancercelllines; CVCL_8756
DR   IARC_TP53; 203
DR   Wikidata; Q54951537
RX   PubMed=2253215;
RX   PubMed=2917357;
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Arg282Trp (c.844C>T); ClinVar=VCV000012364; Zygosity=Unspecified (PubMed=2253215).
DI   NCIt; C5673; Colorectal adenoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   59Y
CA   Cancer cell line
DT   Created: 04-04-12; Last updated: 19-12-24; Version: 12
//
RX   PubMed=2253215;
RA   Baker S.J., Preisinger A.C., Jessup J.M., Paraskeva C., Markowitz S.D.,
RA   Willson J.K.V., Hamilton S.R., Vogelstein B.;
RT   "p53 gene mutations occur in combination with 17p allelic deletions as
RT   late events in colorectal tumorigenesis.";
RL   Cancer Res. 50:7717-7722(1990).
//
RX   PubMed=2917357;
RA   Paraskeva C., Finerty S., Mountford R.A., Powell S.C.;
RT   "Specific cytogenetic abnormalities in two new human colorectal
RT   adenoma-derived epithelial cell lines.";
RL   Cancer Res. 49:1282-1286(1989).
//