"Ambry Genetics"[submitter] AND "MST1R"[gene] - ClinVar

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Items: 50

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2395114	NM_002447.4(MST1R):c.4171C>T (p.Arg1391Trp)	MST1R (R1342W +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2324909	NM_002447.4(MST1R):c.4154G>T (p.Gly1385Val)	MST1R (G1336V +2 more)	Single nucleotide variant (missense variant +1 more)	MST1R-related condition +1 more	GConflicting classifications of pathogenicity
Select item 2491557	NM_002447.4(MST1R):c.4141T>C (p.Ser1381Pro)	MST1R (S1275P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2472967	NM_002447.4(MST1R):c.4042C>A (p.Leu1348Met)	MST1R (L1242M +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2592365	NM_002447.4(MST1R):c.3914G>A (p.Arg1305His)	MST1R (R1199H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2495095	NM_002447.4(MST1R):c.3910C>T (p.Arg1304Trp)	MST1R (R1198W +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2229464	NM_002447.4(MST1R):c.3764C>T (p.Ala1255Val)	MST1R (A1206V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2518499	NM_002447.4(MST1R):c.3749C>T (p.Pro1250Leu)	MST1R (P1201L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2345630	NM_002447.4(MST1R):c.3743G>A (p.Arg1248His)	MST1R (R1142H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2524697	NM_002447.4(MST1R):c.3694G>A (p.Asp1232Asn)	MST1R (D1126N +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2404258	NM_002447.4(MST1R):c.3580C>T (p.Arg1194Cys)	MST1R (R1088C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2215922	NM_002447.4(MST1R):c.3578C>T (p.Ala1193Val)	MST1R (A1087V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2342070	NM_002447.4(MST1R):c.3532C>T (p.Arg1178Trp)	MST1R (R1129W +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2363885	NM_002447.4(MST1R):c.3521G>A (p.Arg1174His)	MST1R (R1174H +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2220349	NM_002447.4(MST1R):c.3488A>G (p.Tyr1163Cys)	MST1R (Y1114C +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2515809	NM_002447.4(MST1R):c.3157C>T (p.Arg1053Trp)	MST1R (R1053W +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2312436	NM_002447.4(MST1R):c.3149C>T (p.Pro1050Leu)	MST1R (P1050L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2220618	NM_002447.4(MST1R):c.3120C>G (p.Phe1040Leu)	MST1R (F991L +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2400231	NM_002447.4(MST1R):c.3113C>T (p.Ala1038Val)	MST1R (A932V +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2302153	NM_002447.4(MST1R):c.3082G>A (p.Gly1028Ser)	MST1R (G979S +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2385802	NM_002447.4(MST1R):c.2840G>C (p.Arg947Pro)	MST1R (R841P +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2591102	NM_002447.4(MST1R):c.2839C>T (p.Arg947Trp)	MST1R (R841W +2 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2385071	NM_002447.4(MST1R):c.2779G>A (p.Asp927Asn)	MST1R (D821N +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2271134	NM_002447.4(MST1R):c.2735A>T (p.Asp912Val)	MST1R (D806V +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2514160	NM_002447.4(MST1R):c.2728C>T (p.Arg910Trp)	MST1R (R804W +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2304246	NM_002447.4(MST1R):c.2722G>A (p.Glu908Lys)	MST1R (E908K +1 more)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2357731	NM_002447.4(MST1R):c.2484A>C (p.Glu828Asp)	MST1R (E828D +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2522279	NM_002447.4(MST1R):c.2482G>A (p.Glu828Lys)	MST1R (E722K +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2276176	NM_002447.4(MST1R):c.2416G>A (p.Gly806Arg)	MST1R (G806R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2258083	NM_002447.4(MST1R):c.2142C>G (p.Ser714Arg)	MST1R (S714R +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2492963	NM_002447.4(MST1R):c.1886T>C (p.Val629Ala)	MST1R (V629A +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2212942	NM_002447.4(MST1R):c.1850G>A (p.Arg617Gln)	MST1R (R617Q +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2404215	NM_002447.4(MST1R):c.1814G>A (p.Gly605Glu)	MST1R (G605E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2256341	NM_002447.4(MST1R):c.1784A>G (p.Tyr595Cys)	MST1R (Y489C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2539908	NM_002447.4(MST1R):c.1775C>G (p.Ser592Cys)	MST1R (S592C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2518215	NM_002447.4(MST1R):c.1604G>A (p.Arg535His)	MST1R (R535H +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2515926	NM_002447.4(MST1R):c.1567C>G (p.Gln523Glu)	MST1R (Q417E +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2325090	NM_002447.4(MST1R):c.1499G>A (p.Arg500Gln)	MST1R (R500Q)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2301980	NM_002447.4(MST1R):c.1498C>T (p.Arg500Trp)	MST1R (R500W)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2391528	NM_002447.4(MST1R):c.1304G>A (p.Arg435His)	MST1R (R435H)	Single nucleotide variant (missense variant +2 more)	Inborn genetic diseases	GUncertain significance
Select item 2603336	NM_002447.4(MST1R):c.1208C>T (p.Ser403Leu)	MST1R (S403L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GLikely benign
Select item 2599614	NM_002447.4(MST1R):c.1050T>A (p.Phe350Leu)	MST1R (F350L)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2516816	NM_002447.4(MST1R):c.1043G>A (p.Gly348Glu)	MST1R (G348E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2383373	NM_002447.4(MST1R):c.926G>A (p.Arg309Gln)	MST1R (R309Q)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2290645	NM_002447.4(MST1R):c.581C>A (p.Ala194Asp)	MST1R (A194D)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2610491	NM_002447.4(MST1R):c.509G>C (p.Arg170Pro)	MST1R (R170P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2258367	NM_002447.4(MST1R):c.306G>T (p.Gln102His)	MST1R (Q102H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2239294	NM_002447.4(MST1R):c.267G>C (p.Gln89His)	MST1R (Q89H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2479317	NM_002447.4(MST1R):c.253C>G (p.Leu85Val)	MST1R (L85V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2398406	NM_002447.4(MST1R):c.104C>T (p.Ala35Val)	MST1R (A35V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 50