Variant #0000069080 (NC_000001.10:g.47746678G>C, NM_003035.2:c.1452C>G (STIL))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.47746678G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID STIL_000094
Frequency 2146/13006
Freq. EA 658/8600
Freq. AA 1488/4406
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 18:34:34 +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.1452C>G r.(=) p.(=)