Variant #0000379689 (NC_000003.11:g.50214207A>G, NM_004186.3:c.556A>G (SEMA3F))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.50214207A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SEMA3F_000045
Frequency 24/13006
Freq. EA 22/8600
Freq. AA 2/4406
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 16:23:53 +02:00 (CEST)
Date last edited 2013-05-04 02:13:41 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
SEMA3F NM_004186.3 ?/? c.556A>G r.(?) p.(Ile186Val)