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Cystic fibrosis - Diagnostic v1.6 Arina Puzriakova Panel version 1.5 has been signed off on 2026-08-12
Cystic fibrosis - Diagnostic v1.5 Achchuthan Shanmugasundram Panel name changed from Cystic fibrosis diagnostic test to Cystic fibrosis - Diagnostic
List of related panels changed from R184; GT219; TP46 to Cystic fibrosis diagnostic test; R184; GT219; TP46
Cystic fibrosis - Diagnostic v1.4 Eleanor Williams List of related panels changed from R184 to R184; GT219; TP46
Cystic fibrosis - Diagnostic v1.2 CFTR Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #219700) and the OMIM record was last accessed on 17 December 2025.
Cystic fibrosis - Diagnostic v1.2 CFTR Achchuthan Shanmugasundram Phenotypes for gene: CFTR were changed from to Cystic fibrosis, OMIM:219700; cystic fibrosis, MONDO:0009061
Cystic fibrosis - Diagnostic v1.1 Achchuthan Shanmugasundram Panel version 1.0 has been signed off on 2023-09-14
Cystic fibrosis - Diagnostic v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Cystic fibrosis - Diagnostic v0.3 Achchuthan Shanmugasundram Panel types changed to GMS Rare Disease; GMS signed-off
Cystic fibrosis - Diagnostic v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Cystic fibrosis - Diagnostic v0.1 CFTR Achchuthan Shanmugasundram edited their review of gene: CFTR: Changed rating: GREEN
Cystic fibrosis - Diagnostic v0.1 CFTR Achchuthan Shanmugasundram reviewed gene: CFTR: Rating: ; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Cystic fibrosis - Diagnostic v0.1 CFTR Achchuthan Shanmugasundram gene: CFTR was added
gene: CFTR was added to Cystic fibrosis diagnostic test. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: CFTR was set to BIALLELIC, autosomal or pseudoautosomal
Cystic fibrosis - Diagnostic v0.0 Achchuthan Shanmugasundram Added Panel Cystic fibrosis diagnostic test
Set list of related panels to R184
Set panel types to: GMS Rare Disease