Variant #0001888903 (NC_000021.8:g.43769959G>A, NC_000021.8(NM_005423.4):c.229+31C>T (TFF2))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.43769959G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TFF2_000016
Frequency 1/12996
Freq. EA 0/8596
Freq. AA 1/4400
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.229+31C>T r.(=) p.(=)