Variant #0000714758 (NC_000007.13:g.540170G>A, NC_000007.13(NM_002607.5):c.581-34C>T (PDGFA))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.540170G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PDGFA_000022
Frequency 4/12998
Freq. EA 2/8592
Freq. AA 2/4406
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 2014-05-04 18:20:22 +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.581-34C>T r.(=) p.(=)