"Athena Diagnostics"[submitter] AND "FOXG1"[gene] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 193306	NM_005249.5(FOXG1):c.218A>C (p.Gln73Pro)	FOXG1 (Q73P)	Single nucleotide variant (missense variant)	FOXG1 disorder	GBenign FDA Recognized database
Select item 205469	NM_005249.5(FOXG1):c.245C>A (p.Pro82Gln)	FOXG1 (P82Q)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 158595	NM_005249.5(FOXG1):c.456G>T (p.Gly152=)	FOXG1	Single nucleotide variant (synonymous variant)	FOXG1 disorder	GBenign FDA Recognized database
Select item 471470	NM_005249.5(FOXG1):c.506del (p.Gly169fs)	FOXG1 (G169fs)	Deletion (frameshift variant)	FOXG1 disorder +3 more	GPathogenic
Select item 447353	NM_005249.5(FOXG1):c.501G>A (p.Glu167=)	FOXG1	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 381951	NM_005249.5(FOXG1):c.1203C>T (p.Ser401=)	FOXG1	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 205476	NM_005249.5(FOXG1):c.1273T>C (p.Ser425Pro)	FOXG1 (S425P)	Single nucleotide variant (missense variant)	FOXG1 disorder	GBenign FDA Recognized database
Select item 205477	NM_005249.5(FOXG1):c.1278G>A (p.Met426Ile)	FOXG1 (M426I)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 137392	NM_005249.5(FOXG1):c.1323C>T (p.Ser441=)	FOXG1	Single nucleotide variant (synonymous variant)	FOXG1 disorder	GBenign FDA Recognized database