Variant #0000596207 (NC_000005.9:g.149513403T>C, NC_000005.9(NM_002609.3):c.759+41A>G (PDGFRB))

Chromosome 5
DNA change (genomic) (Relative to hg19 / GRCh37) g.149513403T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID PDGFRB_000208
Frequency 373/13006
Freq. EA 1/8600
Freq. AA 372/4406
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 16:26:58 +02:00 (CEST)
Date last edited 2013-05-04 08:02:37 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
PDGFRB NM_002609.3 ?/? c.759+41A>G r.(=) p.(=)