Variant #0000069055 (NC_000001.10:g.47737772C>T, NM_003035.2:c.2359G>A (STIL))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.47737772C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID STIL_000051
Frequency 2/13006
Freq. EA 2/8600
Freq. AA 0/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2013-05-03 18:34:31 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
STIL NM_003035.2 ?/? c.2359G>A r.(?) p.(Gly787Ser)