Variant #0000596191 (NC_000005.9:g.149512494C>T, NM_002609.3:c.946G>A (PDGFRB))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.149512494C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PDGFRB_000185
Frequency 40/12954
Freq. EA 39/8566
Freq. AA 1/4388
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.946G>A r.(?) p.(Val316Met)