Variant #0001436459 (NC_000016.9:g.107211G>A, NM_024571.3:c.*68G>A (SNRNP25))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.107211G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SNRNP25_000051
Frequency 44/4566
Freq. EA 38/3182
Freq. AA 6/1384
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 16:42:42 +02:00 (CEST)
Date last edited 2014-05-01 03:25:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SNRNP25 NM_024571.3 ?/? c.*68G>A r.(=) p.(=)