Variant #0001861293 (NC_000020.10:g.49626062C>A, NC_000020.10(NM_002237.3):c.774+40G>T (KCNG1))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.49626062C>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KCNG1_000021
Frequency 1/12952
Freq. EA 1/8570
Freq. AA 0/4382
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 05:20:23 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KCNG1 NM_002237.3 ?/? c.774+40G>T r.(=) p.(=)