Variant #0001821936 (NC_000020.10:g.168625_168626insT, NM_001037732.1:c.183_184insA (DEFB128))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.168625_168626insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID DEFB128_000008
Frequency 427/12508
Freq. EA 246/8248
Freq. AA 181/4260
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 16:46:43 +02:00 (CEST)
Date last edited 2014-05-04 13:35:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
DEFB128 NM_001037732.1 ?/? c.183_184insA r.(?) p.(His62Thrfs*5)