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Severe Paediatric Disorders v0.12 SMARCC2 Louise Daugherty reviewed gene: SMARCC2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Severe Paediatric Disorders v0.11 SMARCC2 Louise Daugherty Publications for gene SMARCC2 were updated from to 30847515
Severe Paediatric Disorders v0.10 SMARCC2 Louise Daugherty Added phenotypes Coffin-Siris syndrome 8, 618362 for gene: SMARCC2
Severe Paediatric Disorders v0.9 SMARCC2 Louise Daugherty Added phenotypes Coffin-Siris syndrome 8, 618362 for gene: SMARCC2
Severe Paediatric Disorders v0.9 SMARCC2 Louise Daugherty Added phenotypes Coffin-Siris syndrome 8, 618362 for gene: SMARCC2
Severe Paediatric Disorders v0.8 SMARCC2 Louise Daugherty Added phenotypes Coffin-Siris syndrome 8, 618362 for gene: SMARCC2
Severe Paediatric Disorders v0.8 SMARCC2 Louise Daugherty Mode of inheritance for gene SMARCC2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Added phenotypes Coffin-Siris syndrome 8, 618362 for gene: SMARCC2
Severe Paediatric Disorders v0.7 SMARCC2 Louise Daugherty Source Next Generation Children Project was added to SMARCC2.
Severe Paediatric Disorders v0.5 SMARCC2 Louise Daugherty Source Expert Review Green was added to SMARCC2.
Rating Changed from Red List (low evidence) to Green List (high evidence)
Severe Paediatric Disorders v0.4 SMARCC2 Louise Daugherty gene: SMARCC2 was added
gene: SMARCC2 was added to Severe Paediatric Disorders. Sources: Expert list
Mode of inheritance for gene: SMARCC2 was set to