Variant #0000696237 (NC_000006.11:g.138196813C>T, NC_000006.11(NM_001270507.1):c.487-12C>T (TNFAIP3))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.138196813C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID TNFAIP3_000030
Frequency 2/13006
Freq. EA 1/8600
Freq. AA 1/4406
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 2019-04-09 11:13:05 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
TNFAIP3 NM_001270507.1 ?/? c.487-12C>T r.(=) p.(=)