"Ambry Genetics"[submitter] AND "NEDD9"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2219660	NM_006403.4(NEDD9):c.2476C>T (p.Arg826Cys)	LOC126859587, NEDD9 (R677C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2297454	NM_006403.4(NEDD9):c.2396T>G (p.Leu799Arg)	LOC126859587, NEDD9 (L799R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2554303	NM_006403.4(NEDD9):c.2368A>G (p.Ile790Val)	LOC126859587, NEDD9 (I641V +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2316896	NM_006403.4(NEDD9):c.2318G>A (p.Arg773His)	LOC126859587, NEDD9 (R624H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2495456	NM_006403.4(NEDD9):c.2237G>T (p.Ser746Ile)	LOC126859587, NEDD9 (S597I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2513131	NM_006403.4(NEDD9):c.2221A>C (p.Ile741Leu)	LOC126859587, NEDD9 (I592L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2377819	NM_006403.4(NEDD9):c.2177T>C (p.Ile726Thr)	LOC126859587, NEDD9 (I577T +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2467603	NM_006403.4(NEDD9):c.2152C>T (p.His718Tyr)	LOC126859587, NEDD9 (H718Y +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2320036	NM_006403.4(NEDD9):c.2114G>T (p.Arg705Leu)	LOC126859587, NEDD9 (R705L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2518931	NM_006403.4(NEDD9):c.2086A>C (p.Thr696Pro)	LOC126859587, NEDD9 (T696P +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2557519	NM_006403.4(NEDD9):c.2038G>A (p.Val680Met)	LOC126859587, NEDD9 (V680M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2304328	NM_006403.4(NEDD9):c.1988A>G (p.His663Arg)	NEDD9 (H514R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	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)	Inborn genetic diseases	GUncertain significance
Select item 2468770	NM_006403.4(NEDD9):c.452G>A (p.Gly151Asp)	NEDD9 (G151D)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2535206	NM_006403.4(NEDD9):c.373G>A (p.Gly125Ser)	NEDD9 (G125S)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2240449	NM_006403.4(NEDD9):c.223G>C (p.Glu75Gln)	NEDD9 (E75Q)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2312386	NM_006403.4(NEDD9):c.99A>G (p.Ile33Met)	NEDD9 (I33M)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance

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Items: 34