Variant #0000696238 (NC_000006.11:g.138196817C>G, NC_000006.11(NM_001270507.1):c.487-8C>G (TNFAIP3))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.138196817C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TNFAIP3_000031
Frequency 224/13006
Freq. EA 8/8600
Freq. AA 216/4406
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 16:27:59 +02:00 (CEST)
Date last edited 2013-05-04 10:44:46 +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.487-8C>G r.(=) p.(=)