Variant #0000523450 (NC_000004.11:g.170990252T>G, NC_000004.11(NM_016228.3):c.803+47A>C (AADAT))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.170990252T>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AADAT_000045
Frequency 13/13006
Freq. EA 0/8600
Freq. AA 13/4406
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 16:25:12 +02:00 (CEST)
Date last edited 2018-08-23 00:50:15 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AADAT NM_016228.3 ?/? c.803+47A>C r.(=) p.(=)