Variant #0001888898 (NC_000021.8:g.43767595C>T, NM_005423.4:c.376G>A (TFF2))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.43767595C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TFF2_000011
Frequency 4/13006
Freq. EA 4/8600
Freq. AA 0/4406
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 16:49:50 +02:00 (CEST)
Date last edited 2013-05-06 06:33:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TFF2 NM_005423.4 ?/? c.376G>A r.(?) p.(Asp126Asn)