Variant #0001409062 (NC_000015.9:g.67528764C>T, NM_024666.3:c.343G>A (AAGAB))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.67528764C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAGAB_000062
Frequency 2/12330
Freq. EA 2/8344
Freq. AA 0/3986
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 2018-08-23 04:21:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAGAB NM_024666.3 ?/? c.343G>A r.(?) p.(Asp115Asn)