MUS81[gene] and "single gene"[properties] - ClinVar

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Items: 46

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2327687	NM_025128.5(MUS81):c.34C>A (p.Pro12Thr)	MUS81 (P12T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2526671	NM_025128.5(MUS81):c.43G>T (p.Ala15Ser)	MUS81 (A15S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2263095	NM_025128.5(MUS81):c.100C>G (p.Arg34Gly)	MUS81 (R34G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530345	NM_025128.5(MUS81):c.142C>T (p.Arg48Cys)	MUS81 (R48C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267771	NM_025128.5(MUS81):c.164T>C (p.Leu55Pro)	MUS81 (L55P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297023	NM_025128.5(MUS81):c.167C>T (p.Pro56Leu)	MUS81 (P56L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2558908	NM_025128.5(MUS81):c.271C>G (p.His91Asp)	MUS81 (H91D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611877	NM_025128.5(MUS81):c.278C>T (p.Pro93Leu)	MUS81 (P93L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386386	NM_025128.5(MUS81):c.341C>G (p.Ser114Cys)	MUS81 (S114C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2469355	NM_025128.5(MUS81):c.356C>T (p.Pro119Leu)	MUS81 (P119L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484122	NM_025128.5(MUS81):c.401G>A (p.Arg134Gln)	MUS81 (R134Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2270162	NM_025128.5(MUS81):c.440G>A (p.Arg147Gln)	MUS81 (R147Q)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2612656	NM_025128.5(MUS81):c.524C>A (p.Ala175Asp)	MUS81 (A175D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297019	NM_025128.5(MUS81):c.557G>A (p.Arg186His)	MUS81 (R186H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151178	NM_025128.5(MUS81):c.620C>T (p.Pro207Leu)	MUS81 (P207L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297022	NM_025128.5(MUS81):c.623A>G (p.Glu208Gly)	MUS81 (E208G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151181	NM_025128.5(MUS81):c.707G>A (p.Gly236Glu)	MUS81 (G236E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3297021	NM_025128.5(MUS81):c.788G>A (p.Arg263Lys)	MUS81 (R263K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377709	NM_025128.5(MUS81):c.844G>A (p.Gly282Arg)	MUS81 (G282R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2233672	NM_025128.5(MUS81):c.877C>T (p.Arg293Trp)	MUS81 (R293W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151190	NM_025128.5(MUS81):c.885C>G (p.His295Gln)	MUS81 (H295Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2545816	NM_025128.5(MUS81):c.931G>A (p.Val311Met)	MUS81 (V311M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151195	NM_025128.5(MUS81):c.991A>G (p.Ile331Val)	MUS81 (I331V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2606825	NM_025128.5(MUS81):c.992T>C (p.Ile331Thr)	MUS81 (I331T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2341930	NM_025128.5(MUS81):c.1031T>G (p.Ile344Ser)	MUS81 (I344S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234526	NM_025128.5(MUS81):c.1064G>A (p.Arg355Gln)	MUS81 (R356Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2641973	NM_025128.5(MUS81):c.1077T>C (p.Cys359=)	MUS81	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2590249	NM_025128.5(MUS81):c.1129C>A (p.Leu377Ile)	MUS81 (L377I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 776627	NM_025128.5(MUS81):c.1168A>C (p.Asn390His)	MUS81 (N390H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2519559	NM_025128.5(MUS81):c.1205C>T (p.Thr402Ile)	MUS81 (T402I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2343237	NM_025128.5(MUS81):c.1237G>A (p.Ala413Thr)	MUS81 (A413T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206216	NM_025128.5(MUS81):c.1256T>A (p.Leu419Gln)	MUS81 (L420Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151111	NM_025128.5(MUS81):c.1310G>A (p.Gly437Glu)	MUS81 (G437E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2217806	NM_025128.5(MUS81):c.1330A>G (p.Met444Val)	MUS81 (M445V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151117	NM_025128.5(MUS81):c.1360C>T (p.Leu454Phe)	MUS81 (L454F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3297020	NM_025128.5(MUS81):c.1371T>A (p.Ser457Arg)	MUS81 (S457R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2621374	NM_025128.5(MUS81):c.1391T>C (p.Ile464Thr)	MUS81 (I464T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 285606	NM_025128.5(MUS81):c.1401+1G>T	MUS81	Single nucleotide variant (splice donor variant)	not provided	GUncertain significance
Select item 714046	NM_025128.5(MUS81):c.1409C>T (p.Ser470Leu)	MUS81 (S470L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 2397678	NM_025128.5(MUS81):c.1450G>A (p.Gly484Arg)	MUS81 (G485R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2641974	NM_025128.5(MUS81):c.1477C>T (p.Leu493=)	MUS81	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 3151126	NM_025128.5(MUS81):c.1498C>G (p.Pro500Ala)	MUS81 (P500A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151131	NM_025128.5(MUS81):c.1520A>G (p.Tyr507Cys)	MUS81 (Y507C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2334307	NM_025128.5(MUS81):c.1568T>A (p.Ile523Asn)	MUS81 (I523N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2483451	NM_025128.5(MUS81):c.1625A>G (p.Gln542Arg)	MUS81 (Q542R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2304043	NM_025128.5(MUS81):c.1642G>A (p.Gly548Ser)	MUS81 (G549S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 46