Variant #0000509767 (NC_000004.11:g.123748086C>T, NM_002006.4:c.156C>T (FGF2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.123748086C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FGF2_000006
Frequency 1326/11656
Freq. EA 566/7744
Freq. AA 760/3912
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 16:25:12 +02:00 (CEST)
Date last edited 2013-05-04 05:37:24 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FGF2 NM_002006.4 ?/? c.156C>T r.? p.?