Variant #0000403959 (NC_000013.10:g.33344509G>A, NM_015032.3:c.3875G>A (PDS5B))

Chromosome 13
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification NA
DNA change (genomic) (Relative to hg19 / GRCh37) g.33344509G>A
DNA change (hg38) g.32770371G>A
Published as -
ISCN -
DB-ID PDS5B_000001 See all 5 reported entries
Variant remarks electrophoretic mobility shift assay decreased DNA binding
Reference PubMed: Zhang 2009
ClinVar ID -
dbSNP ID -
Origin In vitro (cloned)
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Johan den Dunnen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Johan den Dunnen
Date created 2010-04-02 14:18:40 +02:00 (CEST)
Date last edited 2020-07-14 21:50:58 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDS5B NM_015032.3 +/. 32 c.3875G>A r.3875g>a p.Arg1292Gln


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