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Date	Panel	Item	Activity
Filter activities 7 actions
16 Apr 2020	Ataxia - paediatric v0.124	SYNGAP1	Zornitza Stark Marked gene: SYNGAP1 as ready
16 Apr 2020	Ataxia - paediatric v0.124	SYNGAP1	Zornitza Stark Gene: syngap1 has been classified as Amber List (Moderate Evidence).
16 Apr 2020	Ataxia - paediatric v0.124	SYNGAP1	Zornitza Stark Publications for gene: SYNGAP1 were set to
16 Apr 2020	Ataxia - paediatric v0.121	SYNGAP1	Zornitza Stark Classified gene: SYNGAP1 as Amber List (moderate evidence)
16 Apr 2020	Ataxia - paediatric v0.121	SYNGAP1	Zornitza Stark Gene: syngap1 has been classified as Amber List (Moderate Evidence).
16 Apr 2020	Ataxia - paediatric v0.120	SYNGAP1	Zornitza Stark reviewed gene: SYNGAP1: Rating: AMBER; Mode of pathogenicity: None; Publications: 26989088; Phenotypes: Mental retardation, autosomal dominant 5, MIM# 612621; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
19 Dec 2019	Ataxia - paediatric v0.0	SYNGAP1	Bryony Thompson gene: SYNGAP1 was added gene: SYNGAP1 was added to Ataxia - paediatric_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: SYNGAP1 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Phenotypes for gene: SYNGAP1 were set to Autosomal dominant mental retardation 5, 612621