Variant #0000016258 (NC_000001.10:g.10042688G>A, NM_022787.3:c.769G>A (NMNAT1))

Chromosome 1
DNA change (genomic) (Relative to hg19 / GRCh37) g.10042688G>A
Reference Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/}
DB-ID NMNAT1_000028
Frequency 14/13006
Freq. EA 11/8600
Freq. AA 3/4406
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 16:20:35 +02:00 (CEST)
Date last edited 2024-04-17 00:21:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

DNA change (cDNA)     

RNA change     

Protein     
NMNAT1 NM_022787.3 ?/? c.769G>A r.(?) p.(Glu257Lys)