Variant #0001369387 (NC_000015.9:g.20644846C>T, NR_036432.1:n.3006G>A (HERC2P3))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.20644846C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HERC2P3_000027
Frequency 1/8416
Freq. EA 0/5398
Freq. AA 1/3018
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 2014-04-28 20:15:46 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HERC2P3 NR_036432.1 ?/? n.3006G>A r.(?) -