Variant #0000403954 (NC_000013.10:g.33232435A>G, NM_015032.3:c.372A>G (PDS5B))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.33232435A>G
DNA change (hg38) g.32658298A>G
Published as -
ISCN -
DB-ID PDS5B_000004 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2301393
Origin Germline
Segregation -
Frequency 0.11-0.49
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.36579 View details
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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PDS5B NM_015032.3 ?/. 4 c.372A>G r.(?) p.(=)


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