Variant #0000880162 (NC_000009.11:g.116800C>G, NM_207305.4:c.1320G>C (FOXD4))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.116800C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FOXD4_000002
Frequency 2408/11856
Freq. EA 1918/7904
Freq. AA 490/3952
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 16:29:58 +02:00 (CEST)
Date last edited 2020-08-31 07:14:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FOXD4 NM_207305.4 ?/? c.1320G>C r.(?) p.(*440Tyrext*55)