Variant #0001249797 (NC_000012.11:g.117318899G>A, NM_003806.1:c.214C>T (HRK))

Chromosome 12
DNA change (genomic) (Relative to hg19 / GRCh37) g.117318899G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HRK_000001
Frequency 126/6732
Freq. EA 3/4734
Freq. AA 123/1998
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 16:39:18 +02:00 (CEST)
Date last edited 2013-05-05 04:35:36 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HRK NM_003806.1 ?/? c.214C>T r.(=) p.(=)