ID   ICC15
AC   CVCL_A1VE
DR   cancercelllines; CVCL_A1VE
DR   Cell_Model_Passport; SIDM01977
DR   DepMap; ACH-001841
DR   Wikidata; Q105509597
CC   Part of: Cancer Dependency Map project (DepMap) (includes Cancer Cell Line Encyclopedia - CCLE).
CC   Sequence variation: Mutation; HGNC; 1101; BRCA2; Simple; p.Asn1718His (c.5152A>C); Zygosity=Unspecified (DepMap=ACH-001841).
CC   Sequence variation: Mutation; HGNC; 1101; BRCA2; Simple; p.Trp2788Ter (c.8363G>A); ClinVar=VCV000052564; Zygosity=Unspecified (DepMap=ACH-001841).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Cys141Tyr (c.422G>A); ClinVar=VCV000140801; Zygosity=Unspecified (DepMap=ACH-001841).
ST   Source(s): DepMap=ACH-001841
ST   Amelogenin: X,Y
ST   CSF1PO: 12
ST   D13S317: 13
ST   D16S539: 10,12
ST   D18S51: 18
ST   D21S11: 31.2,32.2
ST   D3S1358: 17,18
ST   D5S818: 13
ST   D7S820: 11
ST   D8S1179: 10,14
ST   FGA: 24,25
ST   Penta D: 13
ST   Penta E: 13
ST   TH01: 6
ST   TPOX: 8
ST   vWA: 17
DI   NCIt; C35417; Intrahepatic cholangiocarcinoma
DI   ORDO; Orphanet_70567; Cholangiocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
CA   Cancer cell line
DT   Created: 12-01-21; Last updated: 02-05-24; Version: 6
//