Variant #0000379680 (NC_000003.11:g.50212512G>T, NC_000003.11(NM_004186.3):c.457-17G>T (SEMA3F))

Chromosome 3
DNA change (genomic) (Relative to hg19 / GRCh37) g.50212512G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID SEMA3F_000036
Frequency 4546/12992
Freq. EA 2938/8594
Freq. AA 1608/4398
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 02:13:40 +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.457-17G>T r.(=) p.(=)