EPHB3[gene] and "single gene"[properties] - ClinVar

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Items: 47

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3275966	NM_004443.4(EPHB3):c.8G>A (p.Arg3Lys)	EPHB3 (R3K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089674	NM_004443.4(EPHB3):c.67C>G (p.Leu23Val)	EPHB3 (L23V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383275	NM_004443.4(EPHB3):c.107G>A (p.Arg36Gln)	EPHB3 (R36Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2235125	NM_004443.4(EPHB3):c.158C>T (p.Ala53Val)	EPHB3 (A53V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379805	NM_004443.4(EPHB3):c.164C>T (p.Thr55Ile)	EPHB3 (T55I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481485	NM_004443.4(EPHB3):c.215T>C (p.Met72Thr)	EPHB3 (M72T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2567530	NM_004443.4(EPHB3):c.251G>A (p.Arg84His)	EPHB3 (R84H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2349169	NM_004443.4(EPHB3):c.253G>C (p.Glu85Gln)	EPHB3 (E85Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089671	NM_004443.4(EPHB3):c.260G>C (p.Ser87Thr)	EPHB3 (S87T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275962	NM_004443.4(EPHB3):c.299G>A (p.Arg100Gln)	EPHB3 (R100Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370070	NM_004443.4(EPHB3):c.448A>T (p.Met150Leu)	EPHB3 (M150L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614308	NM_004443.4(EPHB3):c.518G>A (p.Arg173His)	EPHB3 (R173H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2295886	NM_004443.4(EPHB3):c.772G>A (p.Gly258Ser)	EPHB3 (G258S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089675	NM_004443.4(EPHB3):c.943G>A (p.Ala315Thr)	EPHB3 (A315T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089676	NM_004443.4(EPHB3):c.977G>A (p.Arg326His)	EPHB3 (R326H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272482	NM_004443.4(EPHB3):c.1079G>A (p.Ser360Asn)	EPHB3 (S360N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275963	NM_004443.4(EPHB3):c.1087C>T (p.Arg363Trp)	EPHB3 (R363W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2270149	NM_004443.4(EPHB3):c.1171C>T (p.Arg391Cys)	EPHB3 (R391C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508911	NM_004443.4(EPHB3):c.1217C>T (p.Thr406Met)	EPHB3 (T406M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542853	NM_004443.4(EPHB3):c.1288G>A (p.Gly430Ser)	EPHB3 (G430S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 767942	NM_004443.4(EPHB3):c.1314G>A (p.Pro438=)	EPHB3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3089665	NM_004443.4(EPHB3):c.1424C>T (p.Pro475Leu)	EPHB3 (P475L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594376	NM_004443.4(EPHB3):c.1432C>T (p.Arg478Trp)	EPHB3 (R478W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 735235	NM_004443.4(EPHB3):c.1491C>T (p.Ile497=)	EPHB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 787261	NM_004443.4(EPHB3):c.1748+4C>T	EPHB3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 2205775	NM_004443.4(EPHB3):c.1781C>T (p.Thr594Met)	EPHB3 (T594M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215302	NM_004443.4(EPHB3):c.1838C>T (p.Thr613Ile)	EPHB3 (T613I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412337	NM_004443.4(EPHB3):c.1888G>A (p.Val630Met)	EPHB3 (V630M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361100	NM_004443.4(EPHB3):c.1917C>G (p.Ile639Met)	EPHB3 (I639M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089667	NM_004443.4(EPHB3):c.1946G>A (p.Arg649His)	EPHB3 (R649H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485526	NM_004443.4(EPHB3):c.1973G>A (p.Arg658Gln)	EPHB3 (R658Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458705	NM_004443.4(EPHB3):c.2015C>T (p.Thr672Ile)	EPHB3 (T672I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 736703	NM_004443.4(EPHB3):c.2031G>C (p.Arg677=)	EPHB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 782245	NM_004443.4(EPHB3):c.2067T>C (p.Phe689=)	EPHB3	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3089668	NM_004443.4(EPHB3):c.2113C>T (p.Arg705Trp)	EPHB3 (R705W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3275964	NM_004443.4(EPHB3):c.2190C>A (p.Phe730Leu)	EPHB3 (F730L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302527	NM_004443.4(EPHB3):c.2251G>C (p.Glu751Gln)	EPHB3 (E751Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089669	NM_004443.4(EPHB3):c.2419C>T (p.Pro807Ser)	EPHB3 (P807S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089670	NM_004443.4(EPHB3):c.2438G>A (p.Arg813Gln)	EPHB3 (R813Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2303977	NM_004443.4(EPHB3):c.2575C>T (p.Pro859Ser)	EPHB3 (P859S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529303	NM_004443.4(EPHB3):c.2588G>C (p.Cys863Ser)	EPHB3 (C863S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254503	NM_004443.4(EPHB3):c.2669A>G (p.Asn890Ser)	EPHB3 (N890S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089672	NM_004443.4(EPHB3):c.2731G>C (p.Gly911Arg)	EPHB3 (G911R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305000	NM_004443.4(EPHB3):c.2773A>C (p.Thr925Pro)	EPHB3 (T925P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2237389	NM_004443.4(EPHB3):c.2783C>T (p.Thr928Met)	EPHB3 (T928M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3089673	NM_004443.4(EPHB3):c.2825A>T (p.Tyr942Phe)	EPHB3 (Y942F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2654327	NM_004443.4(EPHB3):c.2829G>A (p.Lys943=)	EPHB3	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

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Items: 47