Overview

Variant ID 22141
Entrez Gene ID 10735
Gene STAG2 (GeneCards)
Location hg19 X:123125999-123125999
hg38 X:123992149-123992149
Disease Asymptomatic
Method HiSeq X Ten
Mutation(HGVS format) NC_000023.10:g.123125999 C>T (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 155270560

Annotations and predictions

MAF in gnomAD genome (version 2.0.1) 0
CADD Raw score (version 1.3) 0.058827 (Deleterious)
FATHMM raw prediction score 0.07047 (Tolerated)
Deleterious probability by DeFine 0.16 (Neutral)
Entrez Gene ID 10735 (NCBI Gene)
Official Gene Symbol STAG2 (GeneCards)
Number of variants in STAG2 in this database 3 (view all the variants)
Full name stromal antigen 2
Band Xq25
Other IDs Vega: OTTHUMG00000022725
OMIM: 300826
HGNC: HGNC:11355
Ensembl: ENSG00000101972
Other names SA2, SA-2, SCC3B, bA517O1.1
Summary The protein encoded by this gene is a subunit of the cohesin complex, which regulates the separation of sister chromatids during cell division. Targeted inactivation of this gene results in chromatid cohesion defects and aneuploidy, suggesting that genetic disruption of cohesin is a cause of aneuploidy in human cancer. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2013]

Individual #1

Individual ID 29217584.08 (view all the variants in this individual)
Pubmed ID 29217584
Whose mosaic mutation Normal  
Phenotype 1  
Disease Asymptomatic
OMIM ID

Publication #1: 29217584

Pubmed ID 29217584
Title Aging and neurodegeneration are associated with increased mutations in single human neurons.
Journal Science
Publication date 2018.02
Disease Cockayne syndrome Xeroderma Pigmentosum
Number of cases Male cases: 3; Female cases: 6; cases of unknown sex: 15;