Variant #0000771835 (NC_000007.13:g.100806368G>A, NM_003378.3:c.1757C>T (VGF))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.100806368G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID VGF_000006
Frequency 9/12726
Freq. EA 0/8408
Freq. AA 9/4318
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 16:28:58 +02:00 (CEST)
Date last edited 2013-05-04 12:55:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
VGF NM_003378.3 ?/? c.1757C>T r.(?) p.(Ala586Val)