Variant #0001926111 (NC_000022.10:g.37904616G>A, NM_014550.3:c.983C>T (CARD10))

Chromosome 22
DNA change (genomic) (Relative to hg19 / GRCh37) g.37904616G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID CARD10_000158
Frequency 14/12930
Freq. EA 12/8550
Freq. AA 2/4380
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 16:50:05 +02:00 (CEST)
Date last edited 2013-05-06 08:09:52 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
CARD10 NM_014550.3 ?/? c.983C>T r.(?) p.(Ala328Val)