Variant #0001449093 (NC_000016.9:g.2107151T>G, NM_000548.3:c.820T>G (TSC2))
Chromosome |
16 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2107151T>G |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
TSC2_000088 |
Frequency |
1/12296 |
Freq. EA |
1/8124 |
Freq. AA |
0/4172 |
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 07:02:44 +02:00 (CEST) |

Variant on transcripts
|
|