Overview

Variant ID 26016
Entrez Gene ID 2566
Gene GABRG2 (GeneCards)
Location hg19 5:161604911-161604911
hg38 5:162177905-162177905
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000005.9:g.161604911 C>T (Genome Assembly: GRCh37)

Other information

Exon or Intron NA
Position in protein NA
Amino acid changes in protein NA > NA
Position in cDNA NA
Changes in cDNA NA > NA
mRNA accession NA
mRNA length NA
Reference length 180915260

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score -0.3285
CADD Raw score (version 1.3) -0.058353 (Deleterious)
FATHMM raw prediction score 0.07241 (Tolerated)
Deleterious probability by DeFine 0.5638 (Deleterious)
Entrez Gene ID 2566 (NCBI Gene)
Official Gene Symbol GABRG2 (GeneCards)
Number of variants in GABRG2 in this database 18 (view all the variants)
Full name gamma-aminobutyric acid type A receptor gamma2 subunit
Band 5q34
Other IDs Vega: OTTHUMG00000130350
OMIM: 137164
HGNC: HGNC:4087
Ensembl: ENSG00000113327
Other names CAE2, ECA2, GEFSP3
Summary This gene encodes a gamma-aminobutyric acid (GABA) receptor. GABA is the major inhibitory neurotransmitter in the mammlian brain, where it acts at GABA-A receptors, which are ligand-gated chloride channels. GABA-A receptors are pentameric, consisting of proteins from several subunit classes: alpha, beta, gamma, delta and rho. Mutations in this gene have been associated with epilepsy and febrile seizures. Multiple transcript variants encoding different isoforms have been identified for this gene. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217587.03 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID