Variant #0000880180 (NC_000009.11:g.117228G>A, NM_207305.4:c.892C>T (FOXD4))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.117228G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FOXD4_000020
Frequency 13/9986
Freq. EA 12/6802
Freq. AA 1/3184
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 2020-08-30 01:32:36 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
FOXD4 NM_207305.4 ?/? c.892C>T r.(?) p.(His298Tyr)