Variant #0001651878 (NC_000018.9:g.210001G>A, NM_005151.3:c.1195G>A (USP14))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.210001G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID USP14_000074
Frequency 5/13000
Freq. EA 0/8594
Freq. AA 5/4406
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 16:45:07 +02:00 (CEST)
Date last edited 2014-04-28 05:55:58 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
USP14 NM_005151.3 ?/? c.1195G>A r.(?) p.(Val399Ile)