Variant #0000714755 (NC_000007.13:g.540158G>A, NC_000007.13(NM_002607.5):c.581-22C>T (PDGFA))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.540158G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PDGFA_000019
Frequency 702/12998
Freq. EA 240/8592
Freq. AA 462/4406
Average frequency (gnomAD v.2.1.1) -
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by Ivo F.A.C. Fokkema
Date created 2013-05-03 16:28:58 +02:00 (CEST)
Date last edited 2014-05-01 03:20:40 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PDGFA NM_002607.5 ?/? c.581-22C>T r.(=) p.(=)