Variant #0001369356 (NC_000015.9:g.20643831A>G, NC_000015.9(NR_036432.1):n.3519+14T>C (HERC2P3))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.20643831A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID HERC2P3_000004
Frequency 2/12850
Freq. EA 0/8488
Freq. AA 2/4362
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 2014-04-28 02:50:56 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
HERC2P3 NR_036432.1 ?/? n.3519+14T>C r.(=) p.(=)