ID   ICC6
AC   CVCL_A1VF
DR   cancercelllines; CVCL_A1VF
DR   DepMap; ACH-001846
DR   Wikidata; Q105509606
CC   Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Lys132Thr (c.395A>C); ClinVar=VCV000376627; Zygosity=Unspecified (DepMap=ACH-001846).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Cys135Phe (c.404G>T); ClinVar=VCV000376559; Zygosity=Unspecified (DepMap=ACH-001846).
ST   Source(s): DepMap=ACH-001846
ST   Amelogenin: X
ST   CSF1PO: 12,13
ST   D13S317: 12
ST   D16S539: 11,12
ST   D18S51: 13
ST   D21S11: 30
ST   D3S1358: 14,15
ST   D5S818: 11,12
ST   D7S820: 10
ST   D8S1179: 13
ST   FGA: 20,21
ST   Penta D: 15
ST   Penta E: 12,19
ST   TH01: 6,9.3
ST   TPOX: 8
ST   vWA: 14,20
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: 7
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