Variant #0001409091 (NC_000015.9:g.67546979C>T, NM_024666.3:c.-10G>A (AAGAB))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.67546979C>T
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAGAB_000076
Frequency 23/11832
Freq. EA 0/7976
Freq. AA 23/3856
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 11:41:40 +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.-10G>A r.(=) p.(=)