Variant #0001681408 (NC_000019.9:g.306641G>A, NM_017550.1:c.*49C>T (MIER2))
Chromosome |
19 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.306641G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
MIER2_000002 |
Frequency |
1/12074 |
Freq. EA |
1/7990 |
Freq. AA |
0/4084 |
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 16:45:39 +02:00 (CEST) |
Date last edited |
2014-04-28 19:51:00 +02:00 (CEST) |

Variant on transcripts
|
|