Variant #0000482441 (NC_000004.11:g.57221453C>G, NM_181806.2:c.998G>C (AASDH))

Chromosome 4
DNA change (genomic) (Relative to hg19 / GRCh37) g.57221453C>G
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID AASDH_000116
Frequency 3/13006
Freq. EA 2/8600
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 10:50:37 +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.998G>C r.(?) p.(Gly333Ala)