"Revvity Omics, Revvity"[submitter] AND "EPHB4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1789997	NM_004444.5(EPHB4):c.2350A>G (p.Ile784Val)	EPHB4, LOC126860124 (I784V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1324340	NM_004444.5(EPHB4):c.1738C>T (p.Gln580Ter)	EPHB4 (Q580*)	Single nucleotide variant (nonsense)	not provided	GLikely pathogenic
Select item 1776220	NM_004444.5(EPHB4):c.1603C>T (p.Arg535Trp)	EPHB4 (R535W)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +1 more	GUncertain significance
Select item 1324339	NM_004444.5(EPHB4):c.1124dup (p.Asp376fs)	EPHB4 (D376fs)	Duplication (frameshift variant)	not provided	GLikely pathogenic
Select item 1330626	NM_004444.5(EPHB4):c.1017G>T (p.Leu339=)	EPHB4	Single nucleotide variant (synonymous variant)	EPHB4-related disorder +2 more	GBenign/Likely benign
Select item 1324338	NM_004444.5(EPHB4):c.896C>G (p.Ser299Ter)	EPHB4 (S299*)	Single nucleotide variant (nonsense)	not provided	GPathogenic/Likely pathogenic

ClinVar