Variant #0000803090 (NC_000007.13:g.150656690G>A, NM_000238.3:c.442C>T (KCNH2))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.150656690G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KCNH2_000155
Frequency 16/13006
Freq. EA 16/8600
Freq. AA 0/4406
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 16:28:58 +02:00 (CEST)
Date last edited 2017-01-16 03:54:35 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KCNH2 NM_000238.3 ?/? c.442C>T r.(?) p.(Arg148Trp)