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 International |
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) |

Variant on transcripts
|
|