Variant #0001409053 (NC_000015.9:g.67524220G>C, NM_024666.3:c.467C>G (AAGAB))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.67524220G>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAGAB_000045
Frequency 1/12040
Freq. EA 1/8254
Freq. AA 0/3786
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 2024-04-27 01:01:36 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AAGAB NM_024666.3 ?/? c.467C>G r.(?) p.(Ser156Cys)