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

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Items: 63

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3297087	NM_005115.5(MVP):c.40C>T (p.His14Tyr)	MVP (H14Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591873	NM_005115.5(MVP):c.110G>A (p.Arg37Gln)	MVP (R37Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407657	NM_005115.5(MVP):c.145C>T (p.Arg49Cys)	MVP (R49C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2590707	NM_005115.5(MVP):c.167G>A (p.Arg56His)	MVP (R56H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2352709	NM_005115.5(MVP):c.200G>A (p.Arg67Gln)	MVP (R67Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297090	NM_005115.5(MVP):c.241G>T (p.Val81Phe)	MVP (V81F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292337	NM_005115.5(MVP):c.245G>A (p.Arg82Gln)	MVP (R82Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151763	NM_005115.5(MVP):c.305G>A (p.Gly102Glu)	MVP (G102E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151767	NM_005115.5(MVP):c.355A>T (p.Thr119Ser)	MVP (T119S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2337458	NM_005115.5(MVP):c.413T>A (p.Val138Glu)	MVP (V138E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528523	NM_005115.5(MVP):c.454A>C (p.Ile152Leu)	MVP (I152L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151776	NM_005115.5(MVP):c.461G>A (p.Arg154Gln)	MVP (R154Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3151780	NM_005115.5(MVP):c.524G>T (p.Arg175Leu)	MVP (R175L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409982	NM_005115.5(MVP):c.545G>T (p.Cys182Phe)	MVP (C182F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151787	NM_005115.5(MVP):c.571G>A (p.Val191Met)	MVP (V191M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151792	NM_005115.5(MVP):c.599C>G (p.Thr200Arg)	MVP (T200R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151795	NM_005115.5(MVP):c.646G>A (p.Val216Met)	MVP (V216M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2367327	NM_005115.5(MVP):c.695G>A (p.Arg232Gln)	MVP (R232Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243161	NM_005115.5(MVP):c.695G>C (p.Arg232Pro)	MVP (R232P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297086	NM_005115.5(MVP):c.702C>A (p.Asn234Lys)	MVP (N234K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2283246	NM_005115.5(MVP):c.706C>T (p.Arg236Trp)	MVP (R236W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542958	NM_005115.5(MVP):c.748C>G (p.Leu250Val)	MVP (L250V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151809	NM_005115.5(MVP):c.775C>T (p.His259Tyr)	MVP (H259Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 727084	NM_005115.5(MVP):c.784G>C (p.Asp262His)	MVP (D262H)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2219572	NM_005115.5(MVP):c.852T>G (p.Ile284Met)	MVP (I284M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467487	NM_005115.5(MVP):c.856G>A (p.Asp286Asn)	MVP (D286N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151824	NM_005115.5(MVP):c.869C>T (p.Pro290Leu)	MVP (P290L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2306797	NM_005115.5(MVP):c.872A>C (p.Asp291Ala)	MVP (D291A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288122	NM_005115.5(MVP):c.879G>C (p.Lys293Asn)	MVP (K293N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243414	NM_005115.5(MVP):c.928C>T (p.Leu310Phe)	MVP (L310F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151659	NM_005115.5(MVP):c.1030G>C (p.Glu344Gln)	MVP (E344Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151663	NM_005115.5(MVP):c.1078C>T (p.Arg360Cys)	MVP (R360C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2302632	NM_005115.5(MVP):c.1195C>T (p.Arg399Cys)	MVP (R399C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2407304	NM_005115.5(MVP):c.1196G>A (p.Arg399His)	MVP (R399H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325748	NM_005115.5(MVP):c.1208G>C (p.Gly403Ala)	MVP (G403A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151685	NM_005115.5(MVP):c.1243T>A (p.Trp415Arg)	MVP (W415R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151686	NM_005115.5(MVP):c.1340A>G (p.Gln447Arg)	MVP (Q447R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460245	NM_005115.5(MVP):c.1349C>T (p.Ala450Val)	MVP (A450V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151689	NM_005115.5(MVP):c.1372G>A (p.Val458Ile)	MVP (V458I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356975	NM_005115.5(MVP):c.1499T>C (p.Leu500Pro)	MVP (L500P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209492	NM_005115.5(MVP):c.1504G>A (p.Ala502Thr)	MVP (A502T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2214779	NM_005115.5(MVP):c.1520G>A (p.Arg507His)	MVP (R507H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151701	NM_005115.5(MVP):c.1532G>A (p.Arg511His)	MVP (R511H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151704	NM_005115.5(MVP):c.1637A>T (p.His546Leu)	MVP (H480L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376877	NM_005115.5(MVP):c.1711G>A (p.Ala571Thr)	MVP (A505T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324317	NM_005115.5(MVP):c.1789C>T (p.Arg597Cys)	MVP (R597C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238135	NM_005115.5(MVP):c.1823C>A (p.Thr608Asn)	MVP (T542N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2521022	NM_005115.5(MVP):c.1826C>T (p.Ser609Leu)	MVP (S543L +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3151719	NM_005115.5(MVP):c.1867C>T (p.Arg623Trp)	MVP (R623W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2357930	NM_005115.5(MVP):c.1888C>A (p.Gln630Lys)	MVP (Q564K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2269801	NM_005115.5(MVP):c.1967G>A (p.Arg656His)	MVP (R656H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532067	NM_005115.5(MVP):c.1991T>C (p.Ile664Thr)	MVP (I598T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2536163	NM_005115.5(MVP):c.2015C>T (p.Ala672Val)	MVP (A672V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2299434	NM_005115.5(MVP):c.2053C>T (p.Arg685Cys)	MVP (R619C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356140	NM_005115.5(MVP):c.2069G>A (p.Arg690Gln)	MVP (R624Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151741	NM_005115.5(MVP):c.2139C>T (p.Ser713=)	MVP	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2315965	NM_005115.5(MVP):c.2186G>A (p.Arg729His)	MVP (R663H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297088	NM_005115.5(MVP):c.2189C>T (p.Ala730Val)	MVP (A730V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2529389	NM_005115.5(MVP):c.2536T>C (p.Phe846Leu)	MVP (F786L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3151750	NM_005115.5(MVP):c.2560G>C (p.Glu854Gln)	MVP (E794Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471367	NM_005115.5(MVP):c.2591G>A (p.Ser864Asn)	MVP (S804N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297089	NM_005115.5(MVP):c.2596C>T (p.Pro866Ser)	MVP (P806S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2228600	NM_005115.5(MVP):c.2677C>T (p.Arg893Cys)	MVP (R833C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 63