Variant #0001799756 (NC_000019.9:g.51535322G>A, NM_019598.2:c.267C>T (KLK12))

Chromosome 19
DNA change (genomic) (Relative to hg19 / GRCh37) g.51535322G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID KLK12_000053
Frequency 3/12998
Freq. EA 3/8596
Freq. AA 0/4402
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 02:37:41 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
KLK12 NM_019598.2 ?/? c.267C>T r.(=) p.(=)