ID   AP38P(SVT)
AC   CVCL_JG64
DR   JCRB; JCRB3026
DR   JCRB; KURB1432
DR   Wikidata; Q54750237
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; 3582; FANCA; Simple; p.Ser849Phefs*40 (c.2546delC); ClinVar=VCV000408166; Zygosity=Homozygous (from parent cell line).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) [Note=pSVori-].
CC   Discontinued: JCRB; KURB1432; probable.
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
ST   Source(s): JCRB
ST   Amelogenin: X
ST   CSF1PO: 12,15
ST   D13S317: 9
ST   D16S539: 11,14
ST   D5S818: 9,11
ST   D7S820: 10,11
ST   TH01: 6,9
ST   TPOX: 8,11
ST   vWA: 15,17
DI   NCIt; C125702; Fanconi anemia, complementation group A
DI   ORDO; Orphanet_84; Fanconi anemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_JG62 ! AP38P
SX   Female
AG   9Y
CA   Transformed cell line
DT   Created: 15-05-17; Last updated: 05-10-23; Version: 11
//