Variant #0000509803 (NC_000004.11:g.123814074_123814075insC, NM_002006.4:c.*523_*524insC (FGF2))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.123814074_123814075insC
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FGF2_000032
Frequency 5/12520
Freq. EA 5/8254
Freq. AA 0/4266
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 05:37:25 +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.*523_*524insC r.(?) p.(Glu287Glyfs*13)
NUDT6 NM_007083.4 ?/? c.859_860insG r.(?) p.(Glu287Glyfs*13)