Variant #0001369392 (NC_000015.9:g.20645746G>A, NR_036432.1:n.2924C>T (HERC2P3))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.20645746G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HERC2P3_000036
Frequency 2/12662
Freq. EA 0/8334
Freq. AA 2/4328
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 2014-04-04 03:24:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HERC2P3 NR_036432.1 ?/? n.2924C>T r.(?) -