"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "EPHB2"[ - ClinVar

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Items: 41

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 752283	NM_017449.5(EPHB2):c.210C>T (p.Asn70=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 793553	NM_017449.5(EPHB2):c.240C>A (p.Arg80=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 736600	NM_017449.5(EPHB2):c.261C>T (p.His87=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 770326	NM_017449.5(EPHB2):c.510C>T (p.Ser170=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 749379	NM_017449.5(EPHB2):c.561C>T (p.Leu187=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 767661	NM_017449.5(EPHB2):c.624G>A (p.Gln208=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 732340	NM_017449.5(EPHB2):c.657G>A (p.Leu219=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 745924	NM_017449.5(EPHB2):c.681C>T (p.Ile227=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 765593	NM_017449.5(EPHB2):c.726C>T (p.Asn242=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 744998	NM_017449.5(EPHB2):c.732C>T (p.Asp244=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 8533	NM_017449.5(EPHB2):c.835G>T (p.Ala279Ser)	EPHB2 (A279S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 754697	NM_017449.5(EPHB2):c.909T>C (p.Cys303=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 786719	NM_017449.5(EPHB2):c.930C>T (p.Tyr310=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 733391	NM_017449.5(EPHB2):c.981G>A (p.Ala327=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 777746	NM_017449.5(EPHB2):c.1106G>A (p.Arg369Gln)	EPHB2 (R369Q)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 740850	NM_017449.5(EPHB2):c.1185C>T (p.Ile395=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 740174	NM_017449.5(EPHB2):c.1233G>C (p.Val411=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 737959	NM_017449.5(EPHB2):c.1365G>A (p.Ser455=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 711269	NM_017449.5(EPHB2):c.1429G>A (p.Glu477Lys)	EPHB2 (E477K)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 745287	NM_017449.5(EPHB2):c.1476G>A (p.Thr492=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 783133	NM_017449.5(EPHB2):c.1545= (p.Gly515=)	EPHB2	Variation (no sequence alteration +1 more)	not provided	GBenign
Select item 746774	NM_017449.5(EPHB2):c.1689C>A (p.Ile563=)	EPHB2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 722170	NM_017449.5(EPHB2):c.1700+10G>A	EPHB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 736027	NM_017449.5(EPHB2):c.1704G>A (p.Arg568=)	EPHB2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 717437	NM_017449.5(EPHB2):c.1722C>T (p.Asp574=)	EPHB2	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 725446	NM_017449.5(EPHB2):c.1766-9G>T	EPHB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 795120	NM_017449.5(EPHB2):c.1853T>A (p.Ile618Asn)	EPHB2 (I560N +2 more)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 782365	NM_017449.5(EPHB2):c.1888+9C>T	EPHB2	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 786983	NM_017449.5(EPHB2):c.1949T>C (p.Val650Ala)	EPHB2 (V650A +2 more)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 780763	NM_017449.5(EPHB2):c.1956C>T (p.Ile652=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 753406	NM_017449.5(EPHB2):c.2031C>T (p.Phe677=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 8534	NM_017449.5(EPHB2):c.2032G>A (p.Asp678Asn)	EPHB2 (D679N +2 more)	Single nucleotide variant (missense variant)	Prostate cancer/brain cancer susceptibility +1 more	GLikely benign
Select item 724716	NM_017449.5(EPHB2):c.2127C>T (p.Ser709=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 725130	NM_017449.5(EPHB2):c.2226T>C (p.Tyr742=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 735870	NM_017449.5(EPHB2):c.2319C>T (p.Asp773=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 757402	NM_017449.5(EPHB2):c.2355C>T (p.Gly785=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 770842	NM_017449.5(EPHB2):c.2625A>G (p.Gln875=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 738084	NM_017449.5(EPHB2):c.2640A>G (p.Leu880=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 739040	NM_017449.5(EPHB2):c.2697-9C>T	EPHB2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 753989	NM_017449.5(EPHB2):c.2751G>A (p.Thr917=)	EPHB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2422561	NC_000001.10:g.(?_19199339)_(24690861_?)dup	AKR7L, ALDH4A1 +77 more	Duplication	Deficiency of hydroxymethylglutaryl-CoA lyase	GUncertain significance

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Items: 41