Variant #0000714762 (NC_000007.13:g.540518T>C, NC_000007.13(NM_002607.5):c.580+235A>G (PDGFA))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.540518T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PDGFA_000023
Frequency 2398/5722
Freq. EA 1628/3976
Freq. AA 770/1746
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 2014-05-16 13:45:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PDGFA NM_002607.5 ?/? c.580+235A>G r.(=) p.(=)