Variant #0001799896 (NC_000019.9:g.51584951T>C, NM_022046.4:c.98A>G (KLK14))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.51584951T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KLK14_000057
Frequency 5400/12268
Freq. EA 3132/8276
Freq. AA 2268/3992
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.98A>G r.(?) p.(Gln33Arg)