ID   GM27641
AC   CVCL_ZW61
DR   Coriell; GM27641
DR   Wikidata; Q102113918
CC   Sequence variation: Mutation; HGNC; HGNC:20311; CHAMP1; Simple; p.Arg398Ter (c.1192C>T); ClinVar=VCV000208415; Zygosity=Heterozygous; Note=De novo mutation (Coriell=GM27641).
CC   Transformant: NCBI_TaxID; 10376; Epstein-Barr virus (EBV).
CC   Derived from site: In situ; Peripheral blood; UBERON=UBERON_0000178.
DI   NCIt; C163754; Mental retardation, autosomal dominant 40
DI   ORDO; Orphanet_178469; Autosomal dominant non-syndromic intellectual disability
OX   NCBI_TaxID=9606; ! Homo sapiens (Human)
SX   Male
AG   10Y
CA   Transformed cell line
DT   Created: 29-10-20; Last updated: 19-12-24; Version: 7
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