Variant #0000120669 (NC_000001.10:g.153363062C>A, NC_000001.10(NM_002964.4):c.-22-29G>T (S100A8))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.153363062C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID S100A8_000013
Frequency 332/13002
Freq. EA 7/8598
Freq. AA 325/4404
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 19:41:04 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
S100A8 NM_002964.4 ?/? c.-22-29G>T r.(=) p.(=)