"Fulgent Genetics, Fulgent Genetics"[submitter] AND "EPHA2"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 293411	NM_004431.5(EPHA2):c.2374C>A (p.Arg792=)	EPHA2	Single nucleotide variant (synonymous variant)	Cataract 6 multiple types +1 more	GBenign/Likely benign
Select item 293439	NM_004431.5(EPHA2):c.944G>A (p.Arg315Gln)	EPHA2 (R315Q +1 more)	Single nucleotide variant (missense variant)	Cataract 6 multiple types +1 more	GBenign/Likely benign