"Ambry Genetics"[submitter] AND "VSTM2B"[gene] - ClinVar

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Items: 20

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2319465	NM_001146339.2(VSTM2B):c.41C>T (p.Pro14Leu)	VSTM2B (P14L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2622227	NM_001146339.2(VSTM2B):c.55C>T (p.His19Tyr)	VSTM2B (H19Y)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2278584	NM_001146339.2(VSTM2B):c.79G>A (p.Asp27Asn)	VSTM2B (D27N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2411321	NM_001146339.2(VSTM2B):c.142C>T (p.Pro48Ser)	VSTM2B (P2S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2340831	NM_001146339.2(VSTM2B):c.196T>G (p.Trp66Gly)	VSTM2B (W20G +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596688	NM_001146339.2(VSTM2B):c.214C>T (p.Pro72Ser)	VSTM2B (P26S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2280854	NM_001146339.2(VSTM2B):c.334C>T (p.Leu112Phe)	VSTM2B (L66F +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2304174	NM_001146339.2(VSTM2B):c.365A>T (p.Glu122Val)	VSTM2B (E66V +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2534733	NM_001146339.2(VSTM2B):c.433A>C (p.Met145Leu)	VSTM2B (M145L +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2377883	NM_001146339.2(VSTM2B):c.446T>C (p.Leu149Pro)	VSTM2B (L139P +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2398602	NM_001146339.2(VSTM2B):c.481G>A (p.Glu161Lys)	VSTM2B (E161K +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2325771	NM_001146339.2(VSTM2B):c.523G>C (p.Gly175Arg)	VSTM2B (G87R +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485382	NM_001146339.2(VSTM2B):c.530C>A (p.Ala177Asp)	VSTM2B (A131D +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2388751	NM_001146339.2(VSTM2B):c.535G>T (p.Ala179Ser)	VSTM2B (A123S +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2545649	NM_001146339.2(VSTM2B):c.592G>T (p.Gly198Cys)	VSTM2B (G110C +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2325262	NM_001146339.2(VSTM2B):c.602G>C (p.Ser201Thr)	VSTM2B (S191T +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2461843	NM_001146339.2(VSTM2B):c.617G>T (p.Ser206Ile)	VSTM2B (S196I +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2467841	NM_001146339.2(VSTM2B):c.619C>T (p.Pro207Ser)	VSTM2B (P207S +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2494559	NM_001146339.2(VSTM2B):c.694G>A (p.Ala232Thr)	VSTM2B (A186T +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2392240	NM_001146339.2(VSTM2B):c.779G>A (p.Arg260His)	VSTM2B (R204H +4 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 20