ID   17697M
AC   CVCL_WM37
DR   cancercelllines; CVCL_WM37
DR   Cosmic; 852212
DR   IARC_TP53; 20612
DR   Wikidata; Q93300125
RX   PubMed=15195137;
CC   Sequence variation: Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Unspecified (PubMed=15195137).
CC   Sequence variation: Mutation; HGNC; HGNC:11998; TP53; Simple; p.Tyr234Cys (c.701A>G); ClinVar=VCV000127820; Zygosity=Unspecified (PubMed=15195137).
CC   Derived from site: Metastatic; Lymph node; UBERON=UBERON_0000029.
DI   NCIt; C3224; Melanoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   52Y
CA   Cancer cell line
DT   Created: 24-05-19; Last updated: 19-12-24; Version: 9
//
RX   PubMed=15195137; DOI=10.1038/sj.onc.1207780;
RA   Daniotti M., Oggionni M., Ranzani T., Vallacchi V., Campi V.,
RA   Di Stasi D., Della Torre G., Perrone F., Luoni C., Suardi S.,
RA   Frattini M., Pilotti S., Anichini A., Tragni G., Parmiani G.,
RA   Pierotti M.A., Rodolfo M.;
RT   "BRAF alterations are associated with complex mutational profiles in
RT   malignant melanoma.";
RL   Oncogene 23:5968-5977(2004).
//