Variant #0000880166 (NC_000009.11:g.116848_116849insA, NM_207305.4:c.1271_1272insT (FOXD4))

Chromosome 9
DNA change (genomic) (Relative to hg19 / GRCh37) g.116848_116849insA
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID FOXD4_000006
Frequency 185/12102
Freq. EA 3/8020
Freq. AA 182/4082
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 01:23:36 +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.1271_1272insT r.(?) p.(Leu424Phefs*59)