Variant #0000510004 (NC_000004.11:g.124322934_124322936del, NM_001258038.1:c.188_190del (SPRY1))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.124322934_124322936del
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SPRY1_000013
Frequency 3/12520
Freq. EA 0/8254
Freq. AA 3/4266
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 16:25:12 +02:00 (CEST)
Date last edited 2013-05-04 05:37:45 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SPRY1 NM_001258038.1 ?/? c.188_190del r.(?) p.(Ala64del)