NEDD9[gene] and "single gene"[properties] - ClinVar

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Items: 42

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2304328	NM_006403.4(NEDD9):c.1988A>G (p.His663Arg)	NEDD9 (H514R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2338101	NM_006403.4(NEDD9):c.1914G>C (p.Glu638Asp)	NEDD9 (E489D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 710685	NM_006403.4(NEDD9):c.1899C>T (p.His633=)	NEDD9	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign/Likely benign
Select item 3190819	NM_006403.4(NEDD9):c.1894G>A (p.Val632Ile)	NEDD9 (V483I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2256661	NM_006403.4(NEDD9):c.1837C>T (p.Pro613Ser)	NEDD9 (P464S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 785803	NM_006403.4(NEDD9):c.1743C>T (p.His581=)	NEDD9	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3299153	NM_006403.4(NEDD9):c.1709C>T (p.Pro570Leu)	NEDD9 (P421L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2236191	NM_006403.4(NEDD9):c.1694A>G (p.His565Arg)	NEDD9 (H416R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190813	NM_006403.4(NEDD9):c.1588C>G (p.Arg530Gly)	NEDD9 (R381G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 727676	NM_006403.4(NEDD9):c.1511A>G (p.His504Arg)	NEDD9 (H355R +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely benign
Select item 3190809	NM_006403.4(NEDD9):c.1484C>A (p.Ser495Tyr)	NEDD9 (S346Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318065	NM_006403.4(NEDD9):c.1310G>A (p.Cys437Tyr)	NEDD9 (C288Y +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218592	NM_006403.4(NEDD9):c.1279C>A (p.Leu427Ile)	NEDD9 (L278I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190799	NM_006403.4(NEDD9):c.1184C>T (p.Ser395Phe)	NEDD9 (S246F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190796	NM_006403.4(NEDD9):c.1130G>A (p.Arg377Gln)	NEDD9 (R377Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2461134	NM_006403.4(NEDD9):c.1075C>T (p.Arg359Trp)	NEDD9 (R210W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407029	NM_006403.4(NEDD9):c.1054C>A (p.Pro352Thr)	NEDD9 (P352T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190788	NM_006403.4(NEDD9):c.1012C>T (p.Pro338Ser)	NEDD9 (P189S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339270	NM_006403.4(NEDD9):c.997A>T (p.Ser333Cys)	NEDD9 (S333C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190914	NM_006403.4(NEDD9):c.967G>A (p.Val323Ile)	NEDD9 (V323I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190908	NM_006403.4(NEDD9):c.947C>T (p.Ala316Val)	NEDD9 (A316V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2254985	NM_006403.4(NEDD9):c.871G>A (p.Ala291Thr)	NEDD9 (A142T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2562456	NM_006403.4(NEDD9):c.866C>T (p.Pro289Leu)	NEDD9 (P140L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2462385	NM_006403.4(NEDD9):c.811G>C (p.Ala271Pro)	NEDD9 (A122P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2401802	NM_006403.4(NEDD9):c.770C>T (p.Pro257Leu)	NEDD9 (P108L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267862	NM_006403.4(NEDD9):c.739A>G (p.Met247Val)	NEDD9 (M247V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2487755	NM_006403.4(NEDD9):c.713A>C (p.Glu238Ala)	NEDD9 (E89A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190899	NM_006403.4(NEDD9):c.692G>A (p.Arg231Gln)	NEDD9 (R82Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2465141	NM_006403.4(NEDD9):c.664G>A (p.Val222Ile)	NEDD9 (V73I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2289691	NM_006403.4(NEDD9):c.623T>G (p.Ile208Arg)	NEDD9 (I208R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2561860	NM_006403.4(NEDD9):c.593G>A (p.Gly198Asp)	NEDD9 (G49D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252436	NM_006403.4(NEDD9):c.580T>A (p.Ser194Thr)	NEDD9 (S194T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190880	NM_006403.4(NEDD9):c.568G>A (p.Asp190Asn)	NEDD9 (D41N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2468770	NM_006403.4(NEDD9):c.452G>A (p.Gly151Asp)	NEDD9 (G151D)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3190872	NM_006403.4(NEDD9):c.433A>G (p.Thr145Ala)	NEDD9 (T145A)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 3299154	NM_006403.4(NEDD9):c.425T>C (p.Ile142Thr)	NEDD9 (I142T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2535206	NM_006403.4(NEDD9):c.373G>A (p.Gly125Ser)	NEDD9 (G125S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3190867	NM_006403.4(NEDD9):c.359T>C (p.Val120Ala)	NEDD9 (V120A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3299155	NM_006403.4(NEDD9):c.289C>G (p.Pro97Ala)	NEDD9 (P97A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3190856	NM_006403.4(NEDD9):c.224A>T (p.Glu75Val)	NEDD9 (E75V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2240449	NM_006403.4(NEDD9):c.223G>C (p.Glu75Gln)	NEDD9 (E75Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2312386	NM_006403.4(NEDD9):c.99A>G (p.Ile33Met)	NEDD9 (I33M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 42