Variant #0000617189 (NC_000006.11:g.345968T>G, NC_000006.11(NM_020185.3):c.263+40T>G (DUSP22))

Chromosome 6
DNA change (genomic) (Relative to hg19 / GRCh37) g.345968T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID DUSP22_000053
Frequency 8/13006
Freq. EA 0/8600
Freq. AA 8/4406
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 2014-04-28 16:45:25 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
DUSP22 NM_020185.3 ?/? c.263+40T>G r.(=) p.(=)