Overview

Variant ID 34545
Entrez Gene ID 1106
Gene CHD2 (GeneCards)
Location hg19 15:93543663-93543663
hg38 15:93000433-93000433
Disease Asymptomatic
Method Whole Genome Sequencing Ion Torrent PGM Sequencing
Mutation(HGVS format) NC_000015.9:g.93543663 A>G (Genome Assembly: hg19)

Other information

Exon or Intron intron
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 102531392

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
EIGEN score 0.1366
CADD Raw score (version 1.3) 0.160018 (Deleterious)
FATHMM raw prediction score 0.16136 (Tolerated)
Deleterious probability by DeFine 0.4887 (Neutral)
Entrez Gene ID 1106 (NCBI Gene)
Official Gene Symbol CHD2 (GeneCards)
Number of variants in CHD2 in this database 8 (view all the variants)
Full name chromodomain helicase DNA binding protein 2
Band 15q26.1
Other IDs Vega: OTTHUMG00000185958
OMIM: 602119
HGNC: HGNC:1917
Ensembl: ENSG00000173575
Other names EEOC
Summary The CHD family of proteins is characterized by the presence of chromo (chromatin organization modifier) domains and SNF2-related helicase/ATPase domains. CHD genes alter gene expression possibly by modification of chromatin structure thus altering access of the transcriptional apparatus to its chromosomal DNA template. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]

Individual #1

Individual ID 24760347.01 (view all the variants in this individual)
Pubmed ID 24760347
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 24760347

Pubmed ID 24760347
Title Somatic mutations found in the healthy blood compartment of a 115-yr-old woman demonstrate oligoclonal hematopoiesis
Journal Genome Research
Publication date 2014.04
Disease Asymptomatic
Number of cases Female cases: 1;