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
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