"Mayo Clinic Laboratories, Mayo Clinic"[submitter] AND "EPHB4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1313960	NM_004444.5(EPHB4):c.1692-8G>A	EPHB4	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 3379782	NM_004444.5(EPHB4):c.1436C>T (p.Pro479Leu)	EPHB4 (P479L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3379783	NM_004444.5(EPHB4):c.770C>T (p.Pro257Leu)	EPHB4 (P257L)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1753962	NM_004444.5(EPHB4):c.650T>A (p.Val217Glu)	EPHB4 (V217E)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1740536	NM_004444.5(EPHB4):c.442C>T (p.Arg148Trp)	EPHB4 (R148W)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3379784	NM_004444.5(EPHB4):c.7C>A (p.Leu3Ile)	EPHB4, SLC12A9 (L3I)	Single nucleotide variant (missense variant +1 more)	not provided	GUncertain significance

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