Variant #0001354718 (NC_000014.8:g.96848883C>A, NC_000014.8(NM_016472.3):c.258+41C>A (GSKIP))

Chromosome 14
DNA change (genomic) (Relative to hg19 / GRCh37) g.96848883C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID GSKIP_000011
Frequency 1/13002
Freq. EA 0/8600
Freq. AA 1/4402
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 08:32:38 +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.258+41C>A r.(=) p.(=)