Variant #0001169976 (NC_000012.11:g.6346866C>T, NC_000012.11(NM_001769.3):c.622-63C>T (CD9))
| Chromosome |
12 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.6346866C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
CD9_000073 |
| Frequency |
32/4566 |
| Freq. EA |
1/3182 |
| Freq. AA |
31/1384 |
| 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 16:39:18 +02:00 (CEST) |
| Date last edited |
2013-05-05 01:27:02 +02:00 (CEST) |

Variant on transcripts
|
|