ID   ICC12
AC   CVCL_A1VC
DR   cancercelllines; CVCL_A1VC
DR   Cell_Model_Passport; SIDM01981
DR   DepMap; ACH-001838
DR   Wikidata; Q105509591
CC   Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
CC   Sequence variation: Mutation; HGNC; 1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Unspecified (DepMap=ACH-001838).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Pro190Leu (c.569C>T); ClinVar=VCV000418517; Zygosity=Unspecified (DepMap=ACH-001838).
ST   Source(s): DepMap=ACH-001838
ST   Amelogenin: X
ST   CSF1PO: 12
ST   D13S317: 10,14
ST   D16S539: 9
ST   D18S51: 12,18,19
ST   D21S11: 31.2
ST   D3S1358: 14,15
ST   D5S818: 11,13
ST   D7S820: 11
ST   D8S1179: 13,14
ST   FGA: 20,21
ST   Penta D: 12,14
ST   Penta E: 12
ST   TH01: 8
ST   TPOX: 8
ST   vWA: 15,18
DI   NCIt; C35417; Intrahepatic cholangiocarcinoma
DI   ORDO; Orphanet_70567; Cholangiocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
CA   Cancer cell line
DT   Created: 12-01-21; Last updated: 02-05-24; Version: 6
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