Variant #0001436448 (NC_000016.9:g.106629G>A, NC_000016.9(NM_024571.3):c.341+16G>A (SNRNP25))

Chromosome 16
DNA change (genomic) (Relative to hg19 / GRCh37) g.106629G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SNRNP25_000040
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 16:42:42 +02:00 (CEST)
Date last edited 2014-11-21 01:30:16 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SNRNP25 NM_024571.3 ?/? c.341+16G>A r.(=) p.(=)