Variant #0000509813 (NC_000004.11:g.123814308C>T, NM_002006.4:c.*757C>T (FGF2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.123814308C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FGF2_000052
Frequency 1790/13006
Freq. EA 1501/8600
Freq. AA 289/4406
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 16:25:12 +02:00 (CEST)
Date last edited 2013-05-04 05:37:26 +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.*757C>T r.(?) p.(Arg209Gln)
NUDT6 NM_007083.4 ?/? c.626G>A r.(?) p.(Arg209Gln)