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Date	Panel	Item	Activity
Filter activities 4 actions
14 Feb 2022	Deafness and congenital structural abnormalities v1.18	FGFR2	Arina Puzriakova Mode of inheritance for gene: FGFR2 was changed from BOTH monoallelic and biallelic, autosomal or pseudoautosomal to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
14 Feb 2022	Deafness and congenital structural abnormalities v1.17	FGFR2	Arina Puzriakova Tag Q1_22_MOI was removed from gene: FGFR2.
10 Feb 2022	Deafness and congenital structural abnormalities v1.17	FGFR2	Arina Puzriakova Tag Q1_22_MOI tag was added to gene: FGFR2.
14 Oct 2016	Deafness and congenital structural abnormalities	FGFR2	Ellen McDonagh marked FGFR2 as ready