Overview

Variant ID 29655
Entrez Gene ID 64091
Gene POPDC2 (GeneCards)
Location hg19 3:119367114-119367114
hg38 3:119648267-119648267
Disease Autism Spectrum Disorders (view all the variants in this disease)
Method MiSeq
Mutation(HGVS format) NC_000003.11:g.119367114 G>A (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 198022430

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.6229
CADD Raw score (version 1.3) 0.735461 (Deleterious)
FATHMM raw prediction score 0.29201 (Tolerated)
Deleterious probability by DeFine 0.8627 (Deleterious)
Entrez Gene ID 64091 (NCBI Gene)
Official Gene Symbol POPDC2 (GeneCards)
Number of variants in POPDC2 in this database 2 (view all the variants)
Full name popeye domain containing 2
Band 3q13.33
Other IDs Vega: OTTHUMG00000159438
OMIM: 605823
HGNC: HGNC:17648
Ensembl: ENSG00000121577
Other names POP2
Summary This gene encodes a member of the POP family of proteins which contain three putative transmembrane domains. This membrane associated protein is predominantly expressed in skeletal and cardiac muscle, and may have an important function in these tissues. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 28714951.331 (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;