Related gene-specific medical variations for Gene (Select 4739) - ClinVar - NCBI

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Links from Gene

Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3404106	NM_006403.4(NEDD9):c.2293C>T (p.Arg765Trp)	LOC126859587, NEDD9 (R765W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3404098	NM_006403.4(NEDD9):c.2072A>G (p.Gln691Arg)	LOC126859587, NEDD9 (Q691R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3299156	NM_006403.4(NEDD9):c.2185C>T (p.Leu729Phe)	LOC126859587, NEDD9 (L580F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3190831	NM_006403.4(NEDD9):c.2080C>T (p.Pro694Ser)	LOC126859587, NEDD9 (P545S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2656226	NM_006403.4(NEDD9):c.2037C>T (p.Pro679=)	LOC126859587, NEDD9	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2557519	NM_006403.4(NEDD9):c.2038G>A (p.Val680Met)	LOC126859587, NEDD9 (V680M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	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)	not specified	GUncertain significance
Select item 2219660	NM_006403.4(NEDD9):c.2476C>T (p.Arg826Cys)	LOC126859587, NEDD9 (R677C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance