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Date	Panel	Item	Activity
Filter activities 6 actions
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.45	FGFR2	Zornitza Stark Marked gene: FGFR2 as ready
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.45	FGFR2	Zornitza Stark Gene: fgfr2 has been classified as Red List (Low Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.44	FGFR2	Zornitza Stark Classified gene: FGFR2 as Red List (low evidence)
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.44	FGFR2	Zornitza Stark Gene: fgfr2 has been classified as Red List (Low Evidence).
16 Jan 2020	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.43	FGFR2	Zornitza Stark reviewed gene: FGFR2: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None
17 Nov 2019	Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic v0.0	FGFR2	Zornitza Stark gene: FGFR2 was added gene: FGFR2 was added to Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services Mode of inheritance for gene: FGFR2 was set to Unknown