Variant #0001449012 (NC_000016.9:g.2098774C>G, NC_000016.9(NM_000548.3):c.138+20C>G (TSC2))
Chromosome |
16 |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2098774C>G |
Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
DB-ID |
TSC2_000007 |
Frequency |
4/12992 |
Freq. EA |
4/8598 |
Freq. AA |
0/4394 |
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 07:08:51 +02:00 (CEST) |

Variant on transcripts
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