Variant #0001881106 (NC_000021.8:g.34399362G>C, NM_005806.3:c.192G>C (OLIG2))

Chromosome 21
DNA change (genomic) (Relative to hg19 / GRCh37) g.34399362G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID OLIG2_000008
Frequency 8/13000
Freq. EA 6/8598
Freq. AA 2/4402
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 2013-05-06 06:12:54 +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.192G>C r.(=) p.(=)