Variant #0001369346 (NC_000015.9:g.20588658G>T)

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.20588658G>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID chr15_000038
Frequency 6/12840
Freq. EA 0/8478
Freq. AA 6/4362
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
Options




Variant on transcripts

Stop! No variants on transcripts found!