ID   CTSC#446
AC   CVCL_A9WW
SY   CRC-SC#446
DR   cancercelllines; CVCL_A9WW
DR   Wikidata; Q102113753
RX   PubMed=33128777;
CC   Group: Cancer stem cell line.
CC   From: Sant Andrea Hospital; Rome; Italy.
CC   Microsatellite instability: Stable (MSS) (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 172; ACVR1B; Simple; p.Met361Leu (c.1081A>C); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 172; ACVR1B; Simple; p.Glu482Gly (c.1445A>G); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 2514; CTNNB1; Simple; p.Asp412Gly (c.1235A>G); ClinVar=VCV001498964; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 2514; CTNNB1; Simple; p.Arg717His (c.2150G>A); dbSNP=rs753246841; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 16712; FBXW7; Simple; p.Ser142Arg (c.424A>C); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 16712; FBXW7; Simple; p.Ser678Ter (c.2033C>G); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 6407; KRAS; Simple; p.Asp105Val (c.314A>T); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 7989; NRAS; Simple; p.Cys186Tyr (c.557G>A); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 9588; PTEN; Simple; p.His93Arg (c.278A>G); ClinVar=VCV000007848; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 9588; PTEN; Simple; p.Leu182Ser (c.545T>C); ClinVar=VCV000187827; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 6768; SMAD2; Simple; p.Asn34Asp (c.100A>G); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 6768; SMAD2; Simple; p.Leu254Phe (c.760C>T); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11204; SOX9; Simple; p.Pro108His (c.323C>A); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11641; TCF7L2; Simple; p.Gln263Arg (c.788A>G); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Ala189Profs*58 (c.565delG); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Phe270Cys (c.809T>G); ClinVar=VCV000376597; Zygosity=Unspecified (PubMed=33128777).
CC   Derived from site: In situ; Colon, proximal; UBERON=UBERON_0008972.
ST   Source(s): PubMed=33128777
ST   Amelogenin: X
ST   CSF1PO: 11
ST   D13S317: 9,12
ST   D16S539: 11,13
ST   D5S818: 13
ST   D7S820: 10,11
ST   TH01: 9.3
ST   TPOX: 8,11
ST   vWA: 17
DI   NCIt; C4349; Colon adenocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   87Y
CA   Cancer cell line
DT   Created: 29-10-20; Last updated: 05-10-23; Version: 8
//
RX   PubMed=33128777; DOI=10.1002/ijc.33370;
RA   Visconti P., Parodi F., Parodi B., Casarino L., Romano P.,
RA   Buccarelli M., Pallini R., D'Alessandris Q.G., Montori A., Pilozzi E.,
RA   Ricci-Vitiani L.;
RT   "Short tandem repeat profiling for the authentication of cancer
RT   stem-like cells.";
RL   Int. J. Cancer 148:1489-1498(2021).
//