"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "FOXP4"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 715573	NM_001012426.2(FOXP4):c.456G>A (p.Gln152=)	FOXP4	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2167049	NM_001012426.2(FOXP4):c.814C>T (p.Leu272Phe)	FOXP4 (L271F +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 768090	NM_001012426.2(FOXP4):c.834C>T (p.Pro278=)	FOXP4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 787829	NM_001012426.2(FOXP4):c.1157C>T (p.Pro386Leu)	FOXP4 (P386L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1472670	NM_001012426.2(FOXP4):c.1540G>A (p.Ala514Thr)	FOXP4 (A501T +2 more)	Single nucleotide variant (missense variant)	not provided +8 more	GPathogenic/Likely pathogenic
Select item 768091	NM_001012426.2(FOXP4):c.1788C>T (p.Ser596=)	FOXP4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 719970	NM_001012426.2(FOXP4):c.1789G>A (p.Ala597Thr)	FOXP4 (A584T +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 2422887	NC_000006.11:g.(?_41126341)_(43737486_?)dup	ABCC10, BICRAL +57 more	Duplication	PRPH2-related disorder	GUncertain significance
Select item 2422814	NC_000006.11:g.(?_41126341)_(43752536_?)del	BYSL, CCND3 +58 more	Deletion	Peroxisome biogenesis disorder	GPathogenic

ClinVar