ID   FA17P(SVT)
AC   CVCL_VH75
DR   JCRB; KURB1469
DR   Wikidata; Q54833173
CC   Population: Japanese.
CC   Sequence variation: Mutation; HGNC; 3588; FANCG; Simple; c.307+1G>C (IVS3+1G>C); ClinVar=VCV000006714; Zygosity=Homozygous; Note=Splice donor mutation (from parent cell line).
CC   Transformant: NCBI_TaxID; 1891767; Simian virus 40 (SV40) (Note=pSVori-).
CC   Derived from site: In situ; Skin; UBERON=UBERON_0002097.
CC   Cell type: Fibroblast of skin; CL=CL_0002620.
DI   NCIt; C125708; Fanconi anemia, complementation group G
DI   ORDO; Orphanet_84; Fanconi anemia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
HI   CVCL_VH74 ! FA17P
SX   Male
AG   11Y
CA   Transformed cell line
DT   Created: 14-05-18; Last updated: 10-09-24; Version: 11
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