ID   DD1076
AC   CVCL_9D79
DR   ECACC; 92112018
DR   Wikidata; Q54829519
CC   Part of: ECACC chromosomal abnormality collection.
CC   Karyotypic information: 46,XX,t(1;14)(p34;q22)mat (ECACC=92112018).
CC   Sequence variation: Mutation; HGNC; 1884; CFTR; Simple; p.Gly542Ter (c.1624G>T); ClinVar=VCV000007115; Zygosity=Heterozygous (ECACC=92112018).
CC   Derived from site: In situ; Chorionic villus; UBERON=UBERON_0007106.
DI   NCIt; C2975; Cystic fibrosis
DI   ORDO; Orphanet_586; Cystic fibrosis
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Female
AG   10-11FW
CA   Finite cell line
DT   Created: 23-02-16; Last updated: 29-06-23; Version: 12
//