Variant #0001449072 (NC_000016.9:g.2106610G>T, NC_000016.9(NM_000548.3):c.649-35G>T (TSC2))
Chromosome |
16 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2106610G>T |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
TSC2_000067 |
Frequency |
7/12996 |
Freq. EA |
0/8600 |
Freq. AA |
7/4396 |
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 07:07:19 +02:00 (CEST) |

Variant on transcripts
|
|