Variant #0000880183 (NC_000009.11:g.117485G>C, NM_207305.4:c.635C>G (FOXD4))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.117485G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FOXD4_000025
Frequency 1/11728
Freq. EA 1/7758
Freq. AA 0/3970
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 2020-08-29 15:19:53 +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.635C>G r.(?) p.(Pro212Arg)