"Fulgent Genetics, Fulgent Genetics"[submitter] AND "FOXG1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1046219	NM_005249.5(FOXG1):c.436_438del (p.Glu146del)	FOXG1 (E146del)	Deletion (inframe_deletion)	Rett syndrome, congenital variant	GUncertain significance
Select item 95268	NM_005249.5(FOXG1):c.460dup (p.Glu154fs)	FOXG1 (E154fs)	Duplication (frameshift variant)	FOXG1 disorder	GPathogenic FDA Recognized database
Select item 573079	NM_005249.5(FOXG1):c.1023C>G (p.Tyr341Ter)	FOXG1 (Y341*)	Single nucleotide variant (nonsense)	Rett syndrome, congenital variant	GPathogenic

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