Variant #0000949282 (NC_000009.11:g.135787683G>A, NM_000368.4:c.899C>T (TSC1))
Chromosome |
9 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.135787683G>A |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
TSC1_000121 |
Frequency |
1/13006 |
Freq. EA |
1/8600 |
Freq. AA |
0/4406 |
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 06:59:43 +02:00 (CEST) |

Variant on transcripts
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