Cystic Fibrosis Mutation Database
Also known as CFMDB · CFTR1
The Cystic Fibrosis Mutation Database (CFTR1) was initiated by the Cystic Fibrosis Genetic Analysis Consortium in 1989 to increase and facilitate communications among CF researchers, and is maintained by the Cystic Fibrosis Centre at the Hospital for Sick Children in Toronto. The specific aim of the database is to provide up to date information about individual mutations in the CFTR gene. In a major upgrade in 2010, all known CFTR mutations and sequence variants have been converted to the standard nomenclature recommended by the Human Genome Variation Society.
Getting access
Open access Open
- How to apply
- Not yet verified — we don’t publish a route we haven’t checked.
Summarised from a registry — the exact application route is not yet verified.
About this database
| Website | http://www.genet.sickkids.on.ca/cftr/app |
|---|---|
| Subjects | Life Sciences · Biology · Medicine · Basic Biological and Medical Research · Medicine · General Genetics · Human Genetics |
| Last updated | 2026-09-11 |