Variant #0001651806 (NC_000018.9:g.163266C>G, NC_000018.9(NM_005151.3):c.17-42C>G (USP14))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.163266C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID USP14_000002
Frequency 1/12748
Freq. EA 0/8438
Freq. AA 1/4310
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 20:25:27 +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.17-42C>G r.(=) p.(=)