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Date	Panel	Item	Activity
Filter activities 6 actions
16 Dec 2021	Fetal anomalies v0.1369	COG6	Zornitza Stark Marked gene: COG6 as ready
16 Dec 2021	Fetal anomalies v0.1369	COG6	Zornitza Stark Gene: cog6 has been classified as Green List (High Evidence).
16 Dec 2021	Fetal anomalies v0.1369	COG6	Zornitza Stark Classified gene: COG6 as Green List (high evidence)
16 Dec 2021	Fetal anomalies v0.1369	COG6	Zornitza Stark Gene: cog6 has been classified as Green List (High Evidence).
16 Dec 2021	Fetal anomalies v0.1368	COG6	Zornitza Stark changed review comment from: ID is part of the phenotype.; to: IUGR and microcephaly are a feature.
24 Oct 2021	Fetal anomalies v0.0	COG6	Zornitza Stark gene: COG6 was added gene: COG6 was added to Fetal anomalies. Sources: Expert Review Amber,Genomics England PanelApp Mode of inheritance for gene: COG6 was set to BIALLELIC, autosomal or pseudoautosomal Phenotypes for gene: COG6 were set to Congenital disorder of glycosylation, type IIl, 614576; Shaheen syndrome, 615328