ID   SW480-mCherry
AC   CVCL_A9MH
DR   cancercelllines; CVCL_A9MH
DR   CCRID; 1101HUM-PUMC000834
DR   Wikidata; Q108821346
CC   Population: Caucasian.
CC   Sequence variation: Mutation; HGNC; 583; APC; Simple; p.Gln1338Ter (c.4012C>T); ClinVar=VCV000000801; Zygosity=Homozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; 6407; KRAS; Simple; p.Gly12Val (c.35G>T); ClinVar=VCV000012583; Zygosity=Homozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Arg273His (c.818G>A); ClinVar=VCV000012366; Zygosity=Heterozygous (from parent cell line).
CC   Sequence variation: Mutation; HGNC; 11998; TP53; Simple; p.Pro309Ser (c.925C>T); ClinVar=VCV000458575; Zygosity=Heterozygous (from parent cell line).
CC   Transfected with: UniProtKB; X5DSL3; Anaplasma marginale mCherry fluorescent protein.
CC   Derived from site: In situ; Colon; UBERON=UBERON_0001155.
ST   Source(s): CCRID
ST   Amelogenin: X
ST   CSF1PO: 13,14
ST   D12S391: 17
ST   D13S317: 12
ST   D16S539: 13
ST   D18S51: 13
ST   D19S433: 13
ST   D21S11: 30,30.2
ST   D2S1338: 17,24
ST   D3S1358: 15
ST   D5S818: 13
ST   D6S1043: 11,12
ST   D7S820: 8
ST   D8S1179: 13
ST   FGA: 24
ST   Penta E: 10
ST   TH01: 8
ST   TPOX: 11
ST   vWA: 16
DI   NCIt; C4349; Colon adenocarcinoma
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_0546 ! SW480
SX   Male
AG   51Y
CA   Cancer cell line
DT   Created: 23-09-21; Last updated: 05-10-23; Version: 5
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