ID   UKRV-Mel-27
AC   CVCL_A726
DR   BTO; BTO_0005349
DR   cancercelllines; CVCL_A726
DR   Cosmic; 1846721
DR   Cosmic; 2686534
DR   ESTDAB; ESTDAB-238
DR   Wikidata; Q54990624
RX   PubMed=23348503;
CC   Sequence variation: Mutation; HGNC; HGNC:1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Unspecified (PubMed=23348503).
CC   Sequence variation: Mutation; HGNC; HGNC:11730; TERT; Simple; c.1-124C>T (c.228C>T) (C228T); Zygosity=Unspecified; Note=In promoter (PubMed=23348503).
ST   Source(s): ESTDAB=ESTDAB-238
ST   Amelogenin: X
ST   CSF1PO: 7,11
ST   D13S317: 10,12
ST   D3S1358: 17
ST   D5S818: 12
ST   D7S820: 10,13
ST   FGA: 22,23.2
ST   TH01: 7
ST   TPOX: 8,11
ST   vWA: 17
DI   NCIt; C3224; Melanoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Sex unspecified
AG   Age unspecified
CA   Cancer cell line
DT   Created: 06-06-12; Last updated: 19-12-24; Version: 16
//
RX   PubMed=23348503; DOI=10.1126/science.1230062;
RA   Horn S., Figl A., Rachakonda P.S., Fischer C., Sucker A., Gast A.,
RA   Kadel S., Moll I., Nagore E., Hemminki K., Schadendorf D., Kumar R.;
RT   "TERT promoter mutations in familial and sporadic melanoma.";
RL   Science 339:959-961(2013).
//