Activity

Filter

Cancel
Date Panel Item Activity
6 actions
Inherited MMR deficiency (Lynch syndrome) v1.8 MSH6 Arina Puzriakova Phenotypes for gene: MSH6 were changed from to Colorectal cancer, hereditary nonpolyposis, type 5, OMIM:614350; Colorectal cancer, hereditary nonpolyposis, type 5, MONDO:0013710; Lynch syndrome 1, MONDO:0007356
Inherited MMR deficiency (Lynch syndrome) v0.11 MSH6 Ivone Leong commented on gene: MSH6
Inherited MMR deficiency (Lynch syndrome) v0.8 MSH6 Ivone Leong Mode of inheritance for gene: MSH6 was changed from to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Inherited MMR deficiency (Lynch syndrome) v0.3 MSH6 Rachel Robinson reviewed gene: MSH6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance: ; Current diagnostic: yes
Inherited MMR deficiency (Lynch syndrome) v0.3 MSH6 Lara Hawkes reviewed gene: MSH6: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Inherited MMR deficiency (Lynch syndrome) v0.2 MSH6 Ivone Leong gene: MSH6 was added
gene: MSH6 was added to Inherited MMR deficiency (Lynch syndrome). Sources: Expert List,Expert Review Green,NHS GMS
Mode of inheritance for gene: MSH6 was set to