Variant #0000949314 (NC_000009.11:g.135802555C>T, NC_000009.11(NM_000368.4):c.210+33G>A (TSC1))
| Chromosome |
9 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135802555C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
TSC1_000153 |
| Frequency |
97/13006 |
| Freq. EA |
88/8600 |
| Freq. AA |
9/4406 |
| 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 16:29:58 +02:00 (CEST) |
| Date last edited |
2018-08-23 06:06:14 +02:00 (CEST) |

Variant on transcripts
|
|