Variant #0001409042 (NC_000015.9:g.67500993G>A, NM_024666.3:c.622C>T (AAGAB))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.67500993G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAGAB_000020
Frequency 4/12082
Freq. EA 3/8258
Freq. AA 1/3824
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 2024-04-26 17:48:02 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAGAB NM_024666.3 ?/? c.622C>T r.(?) p.(Pro208Ser)