ID   C14
AC   CVCL_HE29
DR   ColonAtlas; C14
DR   Cosmic; 986003
DR   Wikidata; Q54807856
RX   PubMed=9482574;
CC   Sequence variation: Mutation; HGNC; HGNC:583; APC; Simple; p.Ser1335Lysfs*9 (c.3997_4003dup); Zygosity=Unspecified (PubMed=9482574).
DI   NCIt; C4349; Colon adenocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Cancer cell line
DT   Created: 01-12-16; Last updated: 19-12-24; Version: 6
//
RX   PubMed=9482574; DOI=10.1002/(SICI)1098-1004(1998)11:2<114::AID-HUMU3>3.0.CO;2-J;
RA   Homfray T.F.R., Cottrell S.E., Ilyas M., Rowan A.J., Talbot I.C.,
RA   Bodmer W.F., Tomlinson I.P.M.;
RT   "Defects in mismatch repair occur after APC mutations in the
RT   pathogenesis of sporadic colorectal tumours.";
RL   Hum. Mutat. 11:114-120(1998).
//