ID   ICC3
AC   CVCL_A1ZB
DR   cancercelllines; CVCL_A1ZB
DR   Cell_Model_Passport; SIDM01979
DR   DepMap; ACH-001843
DR   Wikidata; Q105509600
CC   Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
CC   Sequence variation: Mutation; HGNC; 11110; ARID1A; Simple; p.Ala615fs (c.1843_1844insC); Zygosity=Homozygous (DepMap).
CC   Sequence variation: Mutation; HGNC; 2514; CTNNB1; Simple; p.Ser33Pro (c.97T>C); ClinVar=VCV000376391; Zygosity=Heterozygous (DepMap).
CC   Sequence variation: Mutation; HGNC; 6407; KRAS; Simple; p.Gly12Asp (c.35G>A); ClinVar=VCV000012582; Zygosity=Heterozygous (DepMap).
ST   Source(s): DepMap
ST   Amelogenin: X
ST   CSF1PO: 9,10
ST   D13S317: 12,14
ST   D16S539: 11,12
ST   D18S51: 12
ST   D21S11: 27,28
ST   D3S1358: 14,15
ST   D5S818: 10,12
ST   D7S820: 7,11
ST   D8S1179: 12,14
ST   FGA: 20,23
ST   Penta D: 10,12
ST   Penta E: 5,12
ST   TH01: 6,9.3
ST   TPOX: 8
ST   vWA: 14,18
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: 05-10-23; Version: 5
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