Variant #0000120623 (NC_000001.10:g.153333263C>T, NM_002965.3:c.294C>T (S100A9))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.153333263C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID S100A9_000020
Frequency 5/13006
Freq. EA 4/8600
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 19:41:02 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
S100A9 NM_002965.3 ?/? c.294C>T r.(=) p.(=)