Variant #0000596192 (NC_000005.9:g.149512495G>A, NM_002609.3:c.945C>T (PDGFRB))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.149512495G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PDGFRB_000186
Frequency 28/12952
Freq. EA 0/8564
Freq. AA 28/4388
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 16:26:58 +02:00 (CEST)
Date last edited 2013-05-04 08:02:35 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRB NM_002609.3 ?/? c.945C>T r.(=) p.(=)