Variant #0000696236 (NC_000006.11:g.138196799_138196800insT, NC_000006.11(NM_001270507.1):c.487-26_487-25insT (TNFAIP3))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.138196799_138196800insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TNFAIP3_000029
Frequency 4/12518
Freq. EA 1/8254
Freq. AA 3/4264
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 16:27:59 +02:00 (CEST)
Date last edited 2019-04-09 10:34:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TNFAIP3 NM_001270507.1 ?/? c.487-26_487-25insT r.(=) p.(=)