Variant #0001560946 (NC_000017.10:g.12921041T>C, NM_001165962.1:c.224A>G (ELAC2))

Chromosome 17
DNA change (genomic) (Relative to hg19 / GRCh37) g.12921041T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID ELAC2_000207
Frequency 1/12986
Freq. EA 1/8590
Freq. AA 0/4396
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 16:44:12 +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.224A>G r.(?) p.(Tyr75Cys)