"Fulgent Genetics, Fulgent Genetics"[submitter] AND "GATA4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 472776	NM_001308093.3(GATA4):c.263G>T (p.Gly88Val)	GATA4 (G88V)	Single nucleotide variant (missense variant +1 more)	Atrial septal defect 2 +6 more	GUncertain significance
Select item 1372032	NM_001308093.3(GATA4):c.623T>C (p.Met208Thr)	GATA4 (M1T +2 more)	Single nucleotide variant (missense variant +1 more)	Cardiovascular phenotype +6 more	GUncertain significance
Select item 472784	NM_001308093.3(GATA4):c.942G>T (p.Glu314Asp)	GATA4 (E313D +3 more)	Single nucleotide variant (missense variant)	Atrial septal defect 2 +6 more	GUncertain significance
Select item 1314160	NM_001308093.3(GATA4):c.1149G>A (p.Gln383=)	GATA4	Single nucleotide variant (synonymous variant)	Atrioventricular septal defect 4 +5 more	GUncertain significance
Select item 239099	NM_001308093.3(GATA4):c.1235C>T (p.Ala412Val)	GATA4 (A411V +3 more)	Single nucleotide variant (missense variant)	not provided +6 more	GBenign/Likely benign
Select item 1197085	NM_001308093.3(GATA4):c.1240C>G (p.Pro414Ala)	GATA4 (P165A +3 more)	Single nucleotide variant (missense variant)	Atrioventricular septal defect 4 +5 more	GUncertain significance
Select item 424039	NM_001308093.3(GATA4):c.1315G>A (p.Asp439Asn)	GATA4 (D438N +3 more)	Single nucleotide variant (missense variant)	Atrial septal defect 2 +5 more	GUncertain significance

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