Variant #0001354708 (NC_000014.8:g.96848567dup, NC_000014.8(NM_016472.3):c.-1-17dup (GSKIP))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.96848567dup
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID GSKIP_000002
Frequency 975/12296
Freq. EA 543/8164
Freq. AA 432/4132
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 16:41:19 +02:00 (CEST)
Date last edited 2013-05-05 08:32:37 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
GSKIP NM_016472.3 ?/? c.-1-17dup r.(=) p.(=)