Overview

Variant ID 29778
Entrez Gene ID 2566
Gene GABRG2 (GeneCards)
Location hg19 5:161524765-161524765
hg38 5:162097759-162097759
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method NextSeq500
Mutation(HGVS format) NC_000005.9:g.161524765 C>T (Genome Assembly: hg19)

Other information

Exon or Intron Exon
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 0.7645
CADD Raw score (version 1.3) 6.049657 (Deleterious)
FATHMM raw prediction score 0.98356 (Tolerated)
SIFT score 0 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 1 (Deleterious)
MutatioinAssessor score 2.545 (Deleterious)
PROVEAN score -4.91 (Deleterious)
MetaSVM score 0.428 (Deleterious)
MetaLR score 0.646 (Deleterious)
MCAP score 0.32 (Deleterious)
FitCons score 0.56 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 4.82
PhyloP score based on multiple alignment of 100 vertebrates 7.764
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 16.37
Deleterious probability by iFish2 0.8666 (Deleterious)
Deleterious probability by DeFine 0.9583 (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 28867142.36 (view all the variants in this individual)
Pubmed ID 28867142
Whose mosaic mutation Male Patient  
Origin of mosaic mutation in patients de novo
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28867142

Pubmed ID 28867142
Title Exonic Mosaic Mutations Contribute Risk for Autism Spectrum Disorder
Journal American Journal of Human Genetics
Publication date 2017.08
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 247;