Variant #0001829182 (NC_000020.10:g.5844118G>A, NM_152504.2:c.*9G>A (C20orf196))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.5844118G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID C20orf196_000035
Frequency 2/12996
Freq. EA 2/8594
Freq. AA 0/4402
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 16:46:43 +02:00 (CEST)
Date last edited 2013-05-06 03:56:39 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
C20orf196 NM_152504.2 ?/? c.*9G>A r.(=) p.(=)