CADD is a tool for scoring the deleteriousness of single nucleotide variants as well as insertion/deletions variants in the human genome.
| Database Organization | University of Washington |
| Database Website | https://cadd.gs.washington.edu |
| Location | /fdb/CADD |
| Last Updated | 2024-11-19 |
| Organism | Human |
| Search by keyword | Searches through metadata using keywords |
| Search by filename | Searches through filenames where available |