Variant #0001861286 (NC_000020.10:g.49621176G>T, NM_002237.3:c.942C>A (KCNG1))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.49621176G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KCNG1_000014
Frequency 31/12970
Freq. EA 1/8582
Freq. AA 30/4388
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 05:20:22 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KCNG1 NM_002237.3 ?/? c.942C>A r.(=) p.(=)