Variant #0001651837 (NC_000018.9:g.197599_197600insT, NC_000018.9(NM_005151.3):c.595-17_595-16insT (USP14))

Chromosome 18
DNA change (genomic) (Relative to hg19 / GRCh37) g.197599_197600insT
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID USP14_000033
Frequency 2/12514
Freq. EA 2/8250
Freq. AA 0/4264
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 11:50:36 +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.595-17_595-16insT r.(=) p.(=)