ID   SCC12F-CR2
AC   CVCL_E2W8
RX   PubMed=1312681;
CC   Sequence variation: Mutation; HGNC; 5173; HRAS; Simple; p.Gly12Leu; Zygosity=Unspecified (from parent cell line).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Val216Gly (c.647T>G); ClinVar=VCV000376671; Zygosity=Unspecified (from parent cell line).
CC   Genetic integration: Method=Transfection; Gene=HGNC; 2336; CR2.
CC   Genetic integration: Method=Transfection; Gene=UniProtKB; P00552; Transposon Tn5 neo.
CC   Derived from site: In situ; Face, skin; UBERON=UBERON_1000021.
DI   NCIt; C4819; Skin squamous cell carcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_4028 ! SCC-12F
SX   Male
AG   60Y
CA   Cancer cell line
DT   Created: 10-09-24; Last updated: 10-09-24; Version: 1
//
RX   PubMed=1312681; DOI=10.1038/356347a0;
RA   Li Q.-X., Young L.S., Niedobitek G., Dawson C.W., Birkenbach M.,
RA   Wang F.-H., Rickinson A.B.;
RT   "Epstein-Barr virus infection and replication in a human epithelial
RT   cell system.";
RL   Nature 356:347-350(1992).
//