ID   GM13652
AC   CVCL_1L73
SY   AT128AIV3
DR   CLO; CLO_0032717
DR   BioSample; SAMN00802514
DR   Coriell; GM13652
DR   Wikidata; Q54846688
CC   Sequence variation: Mutation; HGNC; HGNC:795; ATM; Simple; p.Trp57Ter (c.170G>A); ClinVar=VCV000127341; Zygosity=Heterozygous (Coriell=GM13652).
CC   Sequence variation: Mutation; HGNC; HGNC:795; ATM; Simple; p.Arg2547_Ser2549del (c.7638_7646delTAGAATTTC) (7636del9); ClinVar=VCV000003019; Zygosity=Heterozygous (Coriell=GM13652).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C2887; Ataxia telangiectasia syndrome
DI   ORDO; Orphanet_100; Ataxia telangiectasia
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   30Y
CA   Transformed cell line
DT   Created: 08-07-15; Last updated: 19-12-24; Version: 16
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