Overview

Variant ID 22366
Entrez Gene ID 2556
Gene GABRA3 (GeneCards)
Location hg19 X:151491587-151491587
hg38 X:152323115-152323115
Disease Xeroderma Pigmentosum (view all the variants in this disease)
Method HiSeq X Ten
Mutation(HGVS format) NC_000023.10:g.151491587 T>C (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 155270560

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
CADD Raw score (version 1.3) -0.098609 (Deleterious)
FATHMM raw prediction score 0.06559 (Tolerated)
Deleterious probability by DeFine 0.0941 (Neutral)
Entrez Gene ID 2556 (NCBI Gene)
Official Gene Symbol GABRA3 (GeneCards)
Number of variants in GABRA3 in this database 3 (view all the variants)
Full name gamma-aminobutyric acid type A receptor alpha3 subunit
Band Xq28
Other IDs Vega: OTTHUMG00000024183
OMIM: 305660
HGNC: HGNC:4077
Ensembl: ENSG00000011677
Other names None
Summary GABA is the major inhibitory neurotransmitter in the mammalian brain where it acts at GABA-A receptors, which are ligand-gated chloride channels. Chloride conductance of these channels can be modulated by agents such as benzodiazepines that bind to the GABA-A receptor. At least 16 distinct subunits of GABA-A receptors have been identified. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 29217584.23 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Female Patient  
Phenotype 3  
Disease Xeroderma Pigmentosum (view all the variants in this disease)
OMIM ID 278700

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;