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Date	Panel	Item	Activity
Filter activities 11 actions
07 Jun 2026	Regression v1.0	CCDC88C	Gene migrated from ENSG00000015133 to ENSG00000015133 (gene set migration)
28 Dec 2019	Regression v0.27	CCDC88C	Zornitza Stark Mode of inheritance for gene: CCDC88C was changed from BIALLELIC, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
28 Dec 2019	Regression v0.26	CCDC88C	Zornitza Stark Marked gene: CCDC88C as ready
28 Dec 2019	Regression v0.26	CCDC88C	Zornitza Stark Gene: ccdc88c has been classified as Amber List (Moderate Evidence).
28 Dec 2019	Regression v0.26	CCDC88C	Zornitza Stark Mode of inheritance for gene: CCDC88C was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
28 Dec 2019	Regression v0.25	CCDC88C	Zornitza Stark Phenotypes for gene: CCDC88C were changed from to Spinocerebellar ataxia 40, MIM#616053
28 Dec 2019	Regression v0.24	CCDC88C	Zornitza Stark Publications for gene: CCDC88C were set to
28 Dec 2019	Regression v0.23	CCDC88C	Zornitza Stark Classified gene: CCDC88C as Amber List (moderate evidence)
28 Dec 2019	Regression v0.23	CCDC88C	Zornitza Stark Gene: ccdc88c has been classified as Amber List (Moderate Evidence).
28 Dec 2019	Regression v0.22	CCDC88C	Zornitza Stark reviewed gene: CCDC88C: Rating: AMBER; Mode of pathogenicity: None; Publications: 25062847, 30398676; Phenotypes: Spinocerebellar ataxia 40, MIM#616053; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
18 Nov 2019	Regression v0.0	CCDC88C	Zornitza Stark gene: CCDC88C was added gene: CCDC88C was added to Regression_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: CCDC88C was set to Unknown