Variant #0001799722 (NC_000019.9:g.51533289C>T, NC_000019.9(NM_019598.2):c.592-576G>A (KLK12))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.51533289C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KLK12_000019
Frequency 110/4566
Freq. EA 1/3182
Freq. AA 109/1384
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 02:37:38 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KLK12 NM_019598.2 ?/? c.592-576G>A r.(=) p.(=)