"Ambry Genetics"[submitter] AND "VNN2"[gene] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2261581	NM_004665.6(VNN2):c.1552G>A (p.Val518Ile)	VNN2 (V297I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2303312	NM_004665.6(VNN2):c.1544A>C (p.Gln515Pro)	VNN2 (Q294P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546018	NM_004665.6(VNN2):c.1543C>A (p.Gln515Lys)	VNN2 (Q294K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2232932	NM_004665.6(VNN2):c.1480G>A (p.Gly494Arg)	VNN2 (G441R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553958	NM_004665.6(VNN2):c.1477T>C (p.Cys493Arg)	VNN2 (C493R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530913	NM_004665.6(VNN2):c.1465C>G (p.Leu489Val)	VNN2 (L268V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2210593	NM_004665.6(VNN2):c.1388G>A (p.Arg463His)	VNN2 (R410H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239813	NM_004665.6(VNN2):c.1253C>A (p.Pro418Gln)	LOC126859794, VNN2 (P365Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188725	NM_004665.6(VNN2):c.1250G>A (p.Arg417Gln)	LOC126859794, VNN2 (R364Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2337689	NM_004665.6(VNN2):c.1234T>G (p.Leu412Val)	LOC126859794, VNN2 (L359V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188724	NM_004665.6(VNN2):c.1189G>A (p.Glu397Lys)	VNN2 (E344K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3188723	NM_004665.6(VNN2):c.1165G>A (p.Gly389Arg)	VNN2 (G336R +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2569306	NM_004665.6(VNN2):c.1147G>A (p.Val383Ile)	VNN2 (V383I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3188722	NM_004665.6(VNN2):c.1118T>A (p.Met373Lys)	VNN2 (M320K +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2305954	NM_004665.6(VNN2):c.1117A>G (p.Met373Val)	VNN2 (M320V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3332132	NM_004665.6(VNN2):c.1050A>T (p.Glu350Asp)	VNN2 (E350D +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2460102	NM_004665.6(VNN2):c.1016G>T (p.Gly339Val)	VNN2 (G286V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3332130	NM_004665.6(VNN2):c.910G>A (p.Val304Met)	VNN2 (V251M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2570008	NM_004665.6(VNN2):c.856A>C (p.Lys286Gln)	VNN2 (K233Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2295838	NM_004665.6(VNN2):c.721G>T (p.Val241Phe)	VNN2 (V241F +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2597155	NM_004665.6(VNN2):c.629C>T (p.Thr210Met)	VNN2 (T210M +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2242984	NM_004665.6(VNN2):c.457T>C (p.Cys153Arg)	VNN2 (C100R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188727	NM_004665.6(VNN2):c.446G>A (p.Arg149His)	VNN2 (R149H +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2400596	NM_004665.6(VNN2):c.439A>G (p.Asn147Asp)	VNN2 (N147D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2328837	NM_004665.6(VNN2):c.385G>A (p.Ala129Thr)	VNN2 (A129T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393530	NM_004665.6(VNN2):c.221G>A (p.Arg74Gln)	VNN2 (R74Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2613267	NM_004665.6(VNN2):c.191C>T (p.Ala64Val)	VNN2 (A64V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3188726	NM_004665.6(VNN2):c.168G>T (p.Glu56Asp)	VNN2 (E3D +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369819	NM_004665.6(VNN2):c.157C>G (p.Leu53Val)	VNN2 (L53V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2407032	NM_004665.6(VNN2):c.67C>G (p.Gln23Glu)	VNN2 (Q23E)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2280106	NM_004665.6(VNN2):c.48A>G (p.Ile16Met)	VNN2 (I16M)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3332131	NM_004665.6(VNN2):c.7A>G (p.Thr3Ala)	VNN2 (T3A)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance

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Items: 32