"Lifecell International Pvt. Ltd"[submitter] AND "FOXG1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 189612	NM_005249.5(FOXG1):c.256del (p.Gln86fs)	FOXG1 (Q86fs)	Deletion (frameshift variant)	FOXG1 disorder	GPathogenic FDA Recognized database
Select item 2446398	NM_005249.5(FOXG1):c.339del (p.Ala114fs)	FOXG1 (A114fs)	Deletion (frameshift variant)	Rett syndrome, congenital variant	GLikely pathogenic
Select item 2446393	NM_005249.5(FOXG1):c.609_613dup (p.Asn205fs)	FOXG1 (N205fs)	Duplication (frameshift variant)	Rett syndrome, congenital variant	GLikely pathogenic

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