"Fulgent Genetics, Fulgent Genetics"[submitter] AND "FOXP2"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 95608	NM_014491.4(FOXP2):c.510ACA[4] (p.Gln191del)	FOXP2 (Q216del +2 more)	Microsatellite (inframe_deletion +1 more)	Inborn genetic diseases +3 more	GBenign/Likely benign
Select item 95611	NM_014491.4(FOXP2):c.570A>G (p.Gln190=)	FOXP2	Single nucleotide variant (synonymous variant +1 more)	Inborn genetic diseases +3 more	GBenign
Select item 449028	NM_014491.4(FOXP2):c.598-1G>C	FOXP2	Single nucleotide variant (splice acceptor variant +1 more)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 617625	NM_014491.4(FOXP2):c.1426C>T (p.Arg476Ter)	FOXP2 (R475* +3 more)	Single nucleotide variant (nonsense +1 more)	not provided +1 more	GPathogenic/Likely pathogenic
Select item 358607	NM_014491.4(FOXP2):c.1494T>C (p.Tyr498=)	FOXP2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 589674	NM_014491.4(FOXP2):c.1856G>A (p.Ser619Asn)	FOXP2 (S619N +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 792882	NM_014491.4(FOXP2):c.1937A>G (p.Asn646Ser)	FOXP2 (N645S +3 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GLikely benign

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