Variant #0001799901 (NC_000019.9:g.51585978C>T, NC_000019.9(NM_022046.4):c.26+1G>A (KLK14))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.51585978C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KLK14_000062
Frequency 133/12342
Freq. EA 123/8342
Freq. AA 10/4000
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 16:45:39 +02:00 (CEST)
Date last edited 2013-05-06 02:38:03 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KLK14 NM_022046.4 ?/? c.26+1G>A r.spl? p.?