Variant #0000482489 (NC_000004.11:g.57248659T>C, NM_181806.2:c.335A>G (AASDH))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.57248659T>C
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AASDH_000164
Frequency 8/13006
Freq. EA 7/8600
Freq. AA 1/4406
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 09:44:07 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
AASDH NM_181806.2 ?/? c.335A>G r.(?) p.(Glu112Gly)