Variant #0001080636 (NC_000011.9:g.44626627T>C, NM_001024844.1:c.156T>C (CD82))
| Chromosome |
11 |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.44626627T>C |
| Reference |
Copied from the {URL:Exome Variant Server:http://evs.gs.washington.edu/EVS/} |
| DB-ID |
CD82_000023 |
| Frequency |
1/13004 |
| Freq. EA |
1/8598 |
| 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 16:37:25 +02:00 (CEST) |
| Date last edited |
2025-01-02 19:30:30 +01:00 (CET) |

Variant on transcripts
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