Variant #0001560951 (NC_000017.10:g.12921109G>A, NM_001165962.1:c.156C>T (ELAC2))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.12921109G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ELAC2_000212
Frequency 2/12840
Freq. EA 0/8514
Freq. AA 2/4326
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 16:44:12 +02:00 (CEST)
Date last edited 2013-05-05 16:27:23 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
ELAC2 NM_001165962.1 ?/? c.156C>T r.(=) p.(=)