Variant #0001369313 (NC_000015.9:g.20169928C>T)

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.20169928C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID chr15_000005
Frequency 1/12636
Freq. EA 0/8446
Freq. AA 1/4190
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 16:41:46 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts

Stop! No variants on transcripts found!