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Monitoring for G(M)CSF escape mutations v1.2 CSF3R Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #617014) and the OMIM record was last accessed on 20 December 2025.
Monitoring for G(M)CSF escape mutations v1.2 CSF3R Achchuthan Shanmugasundram Phenotypes for gene: CSF3R were changed from to Neutropenia, severe congenital, 7, autosomal recessive, OMIM:617014; autosomal recessive severe congenital neutropenia due to CSF3R deficiency, MONDO:0014865
Monitoring for G(M)CSF escape mutations v1.1 Sarah Leigh Panel version 1.0 has been signed off on 2023-09-14
Monitoring for G(M)CSF escape mutations v1.0 Sarah Leigh promoted panel to version 1.0
Monitoring for G(M)CSF escape mutations v0.3 Sarah Leigh Panel types changed to GMS Rare Disease; GMS signed-off
Monitoring for G(M)CSF escape mutations v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Monitoring for G(M)CSF escape mutations v0.1 CSF3R Achchuthan Shanmugasundram reviewed gene: CSF3R: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Monitoring for G(M)CSF escape mutations v0.1 CSF3R Achchuthan Shanmugasundram gene: CSF3R was added
gene: CSF3R was added to Monitoring for G(M)CSF escape mutations. Sources: NHS GMS,Expert Review Green
Mode of inheritance for gene: CSF3R was set to BIALLELIC, autosomal or pseudoautosomal
Monitoring for G(M)CSF escape mutations v0.0 Achchuthan Shanmugasundram Added Panel Monitoring for G(M)CSF escape mutations
Set list of related panels to R338
Set panel types to: GMS Rare Disease