Related gene-specific medical variations for Gene (Select 144699) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278037	NM_152441.3(FBXL14):c.271A>G (p.Asn91Asp)	FBXL14, LOC130007165 (N91D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2642570	NM_152441.3(FBXL14):c.381C>T (p.Cys127=)	FBXL14, LOC130007165	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign