Variant #0001409032 (NC_000015.9:g.67496528A>G, NC_000015.9(NM_024666.3):c.716-42T>C (AAGAB))

Chromosome 15
DNA change (genomic) (Relative to hg19 / GRCh37) g.67496528A>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AAGAB_000023
Frequency 118/12180
Freq. EA 3/8318
Freq. AA 115/3862
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 10:38:08 +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.716-42T>C r.(=) p.(=)