"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "FBXW11"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2656076	NM_001378974.1(FBXW11):c.1662C>G (p.Pro554=)	FBXW11	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 773465	NM_001378974.1(FBXW11):c.1191C>T (p.Ile397=)	FBXW11	Single nucleotide variant (synonymous variant)	FBXW11-related disorder +1 more	GBenign/Likely benign
Select item 2498993	NM_001378974.1(FBXW11):c.1038C>T (p.His346=)	FBXW11	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3067446	NM_001378974.1(FBXW11):c.971+7G>C	FBXW11	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 873503	NM_001378974.1(FBXW11):c.856T>C (p.Trp286Arg)	FBXW11 (W265R +6 more)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 2656077	NM_001378974.1(FBXW11):c.148-2A>G	FBXW11	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign

ClinVar