Variant #0001369398 (NC_000015.9:g.20645797T>C, NR_036432.1:n.2873A>G (HERC2P3))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.20645797T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HERC2P3_000048
Frequency 147/12942
Freq. EA 0/8546
Freq. AA 147/4396
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 20:05:59 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HERC2P3 NR_036432.1 ?/? n.2873A>G r.(?) -