Variant #0001449080 (NC_000016.9:g.2106669G>A, NM_000548.3:c.673G>A (TSC2))
Chromosome |
16 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2106669G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
TSC2_000075 |
Frequency |
1/12996 |
Freq. EA |
1/8600 |
Freq. AA |
0/4396 |
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 16:42:42 +02:00 (CEST) |
Date last edited |
2018-08-23 07:07:22 +02:00 (CEST) |

Variant on transcripts
|
|