Variant #0001861294 (NC_000020.10:g.49626075G>A, NC_000020.10(NM_002237.3):c.774+27C>T (KCNG1))

Chromosome 20
DNA change (genomic) (Relative to hg19 / GRCh37) g.49626075G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KCNG1_000022
Frequency 13/12980
Freq. EA 0/8584
Freq. AA 13/4396
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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KCNG1 NM_002237.3 ?/? c.774+27C>T r.(=) p.(=)