ID   CTSC#482
AC   CVCL_A9WX
SY   CRC-SC#482
DR   cancercelllines; CVCL_A9WX
DR   Wikidata; Q102113754
RX   PubMed=33128777;
CC   Group: Cancer stem cell line.
CC   From: Sant Andrea Hospital; Rome; Italy.
CC   Microsatellite instability: Instable (MSI-high) (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 583; APC; Simple; p.Asn436Ilefs*18 (c.1307delA); ClinVar=VCV000487058; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 583; APC; Simple; p.Ser1465Trpfs*3 (c.4385_4386AG[4]); ClinVar=VCV000000811; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 583; APC; Simple; p.Asp1636Metfs*14 (c.4906dupG); ClinVar=VCV000469982; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 1097; BRAF; Simple; p.Val600Glu (c.1799T>A); ClinVar=VCV000013961; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 16712; FBXW7; Simple; p.Arg465His (c.1394G>A); ClinVar=VCV000376415; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 8975; PIK3CA; Simple; p.Pro3Thr (c.7C>A); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 8975; PIK3CA; Simple; p.His1047Arg (c.3140A>G); ClinVar=VCV000013652; Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11204; SOX9; Simple; p.Gln368Lys (c.1102C>A); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11204; SOX9; Simple; p.Leu382Gln (c.1145T>A); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Leu201Ter (c.602T>A); Zygosity=Unspecified (PubMed=33128777).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Arg213Gln (c.638G>A); ClinVar=VCV000135359; 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: 12,13
ST   D13S317: 11,12
ST   D16S539: 10
ST   D5S818: 9,10
ST   D7S820: 9,10
ST   TH01: 6,9
ST   TPOX: 8,9,10
ST   vWA: 15,16,17,18
DI   NCIt; C4349; Colon adenocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   63Y
CA   Cancer cell line
DT   Created: 29-10-20; Last updated: 05-10-23; Version: 7
//
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).
//