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Inherited MMR deficiency (Lynch syndrome) v1.7 MLH1 Arina Puzriakova Phenotypes for gene: MLH1 were changed from Colorectal cancer, hereditary nonpolyposis, type 2, OMIM:609310; Colorectal cancer, hereditary nonpolyposis, type 2, MONDO:0012249 to Colorectal cancer, hereditary nonpolyposis, type 2, OMIM:609310; Colorectal cancer, hereditary nonpolyposis, type 2, MONDO:0012249; Lynch syndrome 1, MONDO:0007356
Inherited MMR deficiency (Lynch syndrome) v1.5 MLH1 Arina Puzriakova Phenotypes for gene: MLH1 were changed from to Colorectal cancer, hereditary nonpolyposis, type 2, OMIM:609310; Colorectal cancer, hereditary nonpolyposis, type 2, MONDO:0012249
Inherited MMR deficiency (Lynch syndrome) v0.11 MLH1 Ivone Leong commented on gene: MLH1
Inherited MMR deficiency (Lynch syndrome) v0.6 MLH1 Ivone Leong Mode of inheritance for gene: MLH1 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Inherited MMR deficiency (Lynch syndrome) v0.3 MLH1 Rachel Robinson reviewed gene: MLH1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Inherited MMR deficiency (Lynch syndrome) v0.3 MLH1 Lara Hawkes reviewed gene: MLH1: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Inherited MMR deficiency (Lynch syndrome) v0.2 MLH1 Ivone Leong gene: MLH1 was added
gene: MLH1 was added to Inherited MMR deficiency (Lynch syndrome). Sources: Expert List,Expert Review Green,NHS GMS
Mode of inheritance for gene: MLH1 was set to