Variant #0001881115 (NC_000021.8:g.34399681C>A, NM_005806.3:c.511C>A (OLIG2))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.34399681C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OLIG2_000017
Frequency 2/12852
Freq. EA 2/8502
Freq. AA 0/4350
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 16:49:50 +02:00 (CEST)
Date last edited 2024-04-13 12:21:19 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
OLIG2 NM_005806.3 ?/? c.511C>A r.(=) p.(=)