Variant ID | 999 |
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Entrez Gene ID | 2566 |
Gene | GABRG2 (GeneCards) |
Location | hg19 5:161522518-161522518
hg38 5:162095512-162095512 |
Disease | Human Skin Fibroblasts (view all the variants in this disease) |
Method | HiSeq 2500 |
Mutation(HGVS format) | NC_000005.9:g.161522518 C>T (Genome Assembly: hg19) |
Exon or Intron | Exon |
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Position in protein | 93 |
Amino acid changes in protein | H > Y |
Position in cDNA | NA |
Changes in cDNA | NA > NA |
mRNA accession | NA |
mRNA length | NA |
Reference length | 180915260 |
MAF in gnomAD genome (version 2.0.1) | 0 |
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EIGEN score | 0.3111 |
CADD Raw score (version 1.3) | 5.095876 (Deleterious) |
FATHMM raw prediction score | 0.93556 (Tolerated) |
SIFT score | 0.012 (Deleterious) |
LRT score | 0 (Deleterious) |
MutationTaster score | 1 (Deleterious) |
MutatioinAssessor score | 0.065 (Tolerated) |
PROVEAN score | -1.34 (Tolerated) |
MetaSVM score | -0.144 (Tolerated) |
MetaLR score | 0.331 (Tolerated) |
MCAP score | 0.088 (Deleterious) |
FitCons score | 0.554 (Highly Significant p < 0.003 ) |
Genomic Evolutionary Rate Profiling (GERP) score | 6.07 |
PhyloP score based on multiple alignment of 100 vertebrates | 2.901 |
PhastCons score based on multiple alignment of 100 vertebrates | 1 |
SiPhy log transformed odds ratio on multiple alignment of 29 mammals | 20.644 |
Deleterious probability by iFish2 | 0.2637 (Neutral) |
Deleterious probability by DeFine | 0.8892 (Deleterious) |
Entrez Gene ID | 2566 (NCBI Gene) |
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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 ID | 27788131.02 (view all the variants in this individual) |
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Pubmed ID | 27788131 |
Whose mosaic mutation | Normal |
Phenotype | 1 |
Disease | Human Skin Fibroblasts (view all the variants in this disease) |
OMIM ID | 120353 |
Pubmed ID | 27788131 |
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Title | The Impact of Environmental and Endogenous Damage on Somatic Mutation Load in Human Skin Fibroblasts. |
Journal | PLoS Genetics |
Publication date | 2016.10 |
Disease | Human Skin Fibroblasts |
Population | Caucasian |
Number of cases | Male cases: 2; |