"ITMI"[submitter] AND "FBXW7"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 134380	NM_001349798.2(FBXW7):c.502-2437G>A	FBXW7 (S57N)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134379	NM_001349798.2(FBXW7):c.501+29101T>G	FBXW7 (F45C)	Single nucleotide variant (missense variant +1 more)	not specified	Gnot provided
Select item 134385	NM_001349798.2(FBXW7):c.479C>T (p.Pro160Leu)	FBXW7 (P160L)	Single nucleotide variant (missense variant)	FBXW7-related disorder	GLikely benign
Select item 134384	NM_001349798.2(FBXW7):c.458C>G (p.Pro153Arg)	FBXW7 (P153R)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 134382	NM_001349798.2(FBXW7):c.397A>G (p.Arg133Gly)	FBXW7 (R133G)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 134383	NM_001349798.2(FBXW7):c.58A>G (p.Arg20Gly)	FBXW7 (R20G)	Single nucleotide variant (missense variant)	not specified	Gnot provided
Select item 134381	NM_001349798.2(FBXW7):c.45_46insCCT (p.Thr15_Gly16insPro)	FBXW7	Insertion (inframe_insertion)	not provided	GBenign

ClinVar