Overview

Variant ID 22438
Entrez Gene ID 58155
Gene PTBP2 (GeneCards)
Location hg19 1:97278260-97278260
hg38 1:96812704-96812704
Disease Asymptomatic
Method Single cell Sequencing Cell cloning
Mutation(HGVS format) NC_000001.10:g.97278260 T>G (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 249250621

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.8229
CADD Raw score (version 1.3) 0.091769 (Deleterious)
FATHMM raw prediction score 0.58377 (Tolerated)
Deleterious probability by DeFine 0.6109 (Deleterious)
Entrez Gene ID 58155 (NCBI Gene)
Official Gene Symbol PTBP2 (GeneCards)
Number of variants in PTBP2 in this database 6 (view all the variants)
Full name polypyrimidine tract binding protein 2
Band 1p21.3
Other IDs Vega: OTTHUMG00000010685
OMIM: 608449
HGNC: HGNC:17662
Ensembl: ENSG00000117569
Other names nPTB, PTBLP, brPTB
Summary The protein encoded by this gene binds to intronic polypyrimidine clusters in pre-mRNA molecules and is implicated in controlling the assembly of other splicing-regulatory proteins. This protein is very similar to the polypyrimidine tract binding protein (PTB) but most of its isoforms are expressed primarily in the brain. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Jul 2014]

Individual #1

Individual ID 29217587.01 (view all the variants in this individual)
Pubmed ID 29217587
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217587

Pubmed ID 29217587
Title Different mutational rates and mechanisms in human cells at pregastrulation and neurogenesis.
Journal Science
Publication date 2018.02
Disease Asymptomatic
Number of cases cases of unknown sex: 3;