Variant #0000241696 (NC_000002.11:g.73115631A>C, NM_003124.4:c.493A>C (SPR))

Chromosome 2
DNA change (genomic) (Relative to hg19 / GRCh37) g.73115631A>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SPR_000013
Frequency 4/13006
Freq. EA 0/8600
Freq. AA 4/4406
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 16:22:05 +02:00 (CEST)
Date last edited 2017-02-17 18:50:06 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SPR NM_003124.4 ?/? c.493A>C r.(?) p.(Lys165Gln)