"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "EPHA5"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 787803	NM_001281766.3(EPHA5):c.2235+4G>A	EPHA5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 718434	NM_001281766.3(EPHA5):c.2173+8T>A	EPHA5	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 737306	NM_001281766.3(EPHA5):c.1954T>A (p.Ser652Thr)	EPHA5 (S652T +4 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 716817	NM_001281766.3(EPHA5):c.1938T>C (p.Ala646=)	EPHA5	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 780462	NM_001281766.3(EPHA5):c.1582G>C (p.Glu528Gln)	EPHA5 (E459Q +1 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 787027	NM_001281766.3(EPHA5):c.537C>T (p.Ala179=)	EPHA5	Single nucleotide variant (synonymous variant)	not provided	GBenign

ClinVar