Variant #0001080685 (NC_000011.9:g.44639921C>T, NC_000011.9(NM_001024844.1):c.567+6C>T (CD82))
| Chromosome |
11 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44639921C>T |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
CD82_000072 |
| Frequency |
6350/12956 |
| Freq. EA |
4714/8570 |
| Freq. AA |
1636/4386 |
| 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 16:37:25 +02:00 (CEST) |
| Date last edited |
2013-05-04 22:20:38 +02:00 (CEST) |

Variant on transcripts
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