Variant #0001651881 (NC_000018.9:g.210356_210358del, NC_000018.9(NM_005151.3):c.1226-30_1226-28del (USP14))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.210356_210358del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID USP14_000077
Frequency 76/12512
Freq. EA 52/8248
Freq. AA 24/4264
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 16:45:07 +02:00 (CEST)
Date last edited 2014-04-28 11:50:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
USP14 NM_005151.3 ?/? c.1226-30_1226-28del r.(=) p.(=)