Variant #0000803015 (NC_000007.13:g.150647970C>G, NC_000007.13(NM_000238.3):c.2145+39G>C (KCNH2))

Chromosome 7
DNA change (genomic) (Relative to hg19 / GRCh37) g.150647970C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KCNH2_000080
Frequency 3392/13006
Freq. EA 1999/8600
Freq. AA 1393/4406
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 2013-05-04 13:49:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KCNH2 NM_000238.3 ?/? c.2145+39G>C r.(=) p.(=)