Variant #0001888910 (NC_000021.8:g.43770099C>T, NM_005423.4:c.120G>A (TFF2))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.43770099C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TFF2_000023
Frequency 12/13002
Freq. EA 11/8598
Freq. AA 1/4404
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 06:33:23 +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.120G>A r.(=) p.(=)