Overview

Variant ID 29665
Entrez Gene ID 2802
Gene GOLGA3 (GeneCards)
Location hg19 12:133381371-133381371
hg38 12:132804785-132804785
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method MiSeq
Mutation(HGVS format) NC_000012.11:g.133381371 C>G (Genome Assembly: hg19)

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 133851895

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.4513
CADD Raw score (version 1.3) 2.52852 (Deleterious)
FATHMM raw prediction score 0.97887 (Tolerated)
SIFT score 0.034 (Deleterious)
LRT score 0 (Deleterious)
MutationTaster score 0.999 (Deleterious)
MutatioinAssessor score 1.87 (Tolerated)
PROVEAN score -1.66 (Tolerated)
MetaSVM score -0.041 (Tolerated)
MetaLR score 0.471 (Tolerated)
MCAP score 0.063 (Deleterious)
FitCons score 0.707 (Highly Significant p < 0.003 )
Genomic Evolutionary Rate Profiling (GERP) score 5.52
PhyloP score based on multiple alignment of 100 vertebrates 3.921
PhastCons score based on multiple alignment of 100 vertebrates 1
SiPhy log transformed odds ratio on multiple alignment of 29 mammals 19.43
Deleterious probability by iFish2 0.3708 (Neutral)
Deleterious probability by DeFine 0.9708 (Deleterious)
Entrez Gene ID 2802 (NCBI Gene)
Official Gene Symbol GOLGA3 (GeneCards)
Number of variants in GOLGA3 in this database 2 (view all the variants)
Full name golgin A3
Band 12q24.33
Other IDs Vega: OTTHUMG00000168023
OMIM: 602581
HGNC: HGNC:4426
Ensembl: ENSG00000090615
Other names MEA-2, GCP170
Summary The Golgi apparatus, which participates in glycosylation and transport of proteins and lipids in the secretory pathway, consists of a series of stacked cisternae (flattened membrane sacs). Interactions between the Golgi and microtubules are thought to be important for the reorganization of the Golgi after it fragments during mitosis. This gene encodes a member of the golgin family of proteins which are localized to the Golgi. Its encoded protein has been postulated to play a role in nuclear transport and Golgi apparatus localization. Several alternatively spliced transcript variants that encode different protein isoforms have been described for this gene. [provided by RefSeq, Feb 2010]

Individual #1

Individual ID 28714951.341 (view all the variants in this individual)
Pubmed ID 28714951
Whose mosaic mutation Patient  
Phenotype 3  
Disease Autism Spectrum Disorders (view all the variants in this disease)
OMIM ID 209850

Publication #1: 28714951

Pubmed ID 28714951
Title Rates, distribution and implications of postzygotic mosaic mutations in autism spectrum disorder
Journal Nat Neurosci
Publication date 2017.07
Disease Autism Spectrum Disorders
Incidence 0.01
Number of cases cases of unknown sex: 376;