"Ambry Genetics"[submitter] AND "LNX1"[gene] - ClinVar

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Items: 52

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2591135	NM_030917.4(FIP1L1):c.1730C>T (p.Ala577Val)	FIP1L1, LNX1 (A501V +42 more)	Single nucleotide variant (missense variant +2 more)	not provided +1 more	GUncertain significance
Select item 3095256	NM_030917.4(FIP1L1):c.1761C>G (p.Ser587Arg)	FIP1L1, LNX1 (S522R +42 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2356944	NM_001126328.3(LNX1):c.2158A>T (p.Ile720Phe)	LNX1 (I624F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119488	NM_001126328.3(LNX1):c.2149A>T (p.Thr717Ser)	LNX1 (T621S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2540251	NM_001126328.3(LNX1):c.2101A>C (p.Ile701Leu)	LNX1 (I701L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291036	NM_001126328.3(LNX1):c.2085A>C (p.Arg695Ser)	LNX1 (R599S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291037	NM_001126328.3(LNX1):c.2012T>C (p.Ile671Thr)	LNX1 (I575T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243729	NM_001126328.3(LNX1):c.1964G>A (p.Gly655Glu)	LNX1 (G655E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291039	NM_001126328.3(LNX1):c.1925G>A (p.Arg642Gln)	LNX1 (R642Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119487	NM_001126328.3(LNX1):c.1916T>C (p.Ile639Thr)	LNX1 (I543T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550006	NM_001126328.3(LNX1):c.1787A>G (p.Glu596Gly)	LNX1 (E500G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291038	NM_001126328.3(LNX1):c.1777A>G (p.Lys593Glu)	LNX1 (K593E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119486	NM_001126328.3(LNX1):c.1765G>A (p.Ala589Thr)	LNX1 (A589T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483390	NM_001126328.3(LNX1):c.1712G>A (p.Arg571Gln)	LNX1 (R475Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119484	NM_001126328.3(LNX1):c.1585A>G (p.Arg529Gly)	LNX1 (R529G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253484	NM_001126328.3(LNX1):c.1540C>T (p.Pro514Ser)	LNX1 (P418S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119483	NM_001126328.3(LNX1):c.1436G>A (p.Ser479Asn)	LNX1 (S479N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119482	NM_001126328.3(LNX1):c.1426G>A (p.Gly476Ser)	LNX1 (G476S +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3291041	NM_001126328.3(LNX1):c.1400G>A (p.Arg467Gln)	LNX1 (R371Q +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3119481	NM_001126328.3(LNX1):c.1331G>A (p.Ser444Asn)	LNX1 (S444N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2229404	NM_001126328.3(LNX1):c.1315T>C (p.Tyr439His)	LNX1 (Y343H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2349108	NM_001126328.3(LNX1):c.1208A>G (p.Glu403Gly)	LNX1 (E403G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119480	NM_001126328.3(LNX1):c.1195C>T (p.Arg399Cys)	LNX1 (R399C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2300113	NM_001126328.3(LNX1):c.1186A>G (p.Lys396Glu)	LNX1 (K300E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119479	NM_001126328.3(LNX1):c.1166C>T (p.Pro389Leu)	LNX1 (P293L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291040	NM_001126328.3(LNX1):c.1133A>G (p.Asp378Gly)	LNX1 (D282G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542153	NM_001126328.3(LNX1):c.1127G>A (p.Arg376Gln)	LNX1 (R280Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119478	NM_001126328.3(LNX1):c.1118A>G (p.Tyr373Cys)	LNX1 (Y373C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291525	NM_001126328.3(LNX1):c.1117T>G (p.Tyr373Asp)	LNX1 (Y277D +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291043	NM_001126328.3(LNX1):c.1097A>G (p.Asn366Ser)	LNX1 (N366S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119476	NM_001126328.3(LNX1):c.1069C>T (p.Arg357Cys)	LNX1 (R357C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291035	NM_001126328.3(LNX1):c.1042T>G (p.Cys348Gly)	LNX1 (C252G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119492	NM_001126328.3(LNX1):c.841G>C (p.Asp281His)	LNX1 (D185H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2211414	NM_001126328.3(LNX1):c.836G>A (p.Arg279Gln)	LNX1 (R279Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291042	NM_001126328.3(LNX1):c.796C>G (p.Leu266Val)	LNX1 (L266V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2317636	NM_001126328.3(LNX1):c.773A>G (p.Glu258Gly)	LNX1, LNX1-AS1 (E162G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215724	NM_001126328.3(LNX1):c.708C>G (p.Ser236Arg)	LNX1, LNX1-AS1 (S140R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119491	NM_001126328.3(LNX1):c.673A>T (p.Asn225Tyr)	LNX1, LNX1-AS1 (N129Y +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119490	NM_001126328.3(LNX1):c.646A>G (p.Ile216Val)	LNX1, LNX1-AS1 (I120V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356972	NM_001126328.3(LNX1):c.637A>G (p.Arg213Gly)	LNX1, LNX1-AS1 (R117G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119489	NM_001126328.3(LNX1):c.625C>T (p.Arg209Trp)	LNX1, LNX1-AS1 (R209W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617447	NM_001126328.3(LNX1):c.526G>A (p.Glu176Lys)	LNX1, LNX1-AS1 (E176K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291044	NM_001126328.3(LNX1):c.410C>G (p.Thr137Ser)	LNX1, LNX1-AS1 (T41S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412562	NM_001126328.3(LNX1):c.300G>C (p.Lys100Asn)	LNX1 (K100N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2327641	NM_001126328.3(LNX1):c.281T>A (p.Val94Asp)	LNX1 (V94D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206821	NM_001126328.3(LNX1):c.280G>T (p.Val94Phe)	LNX1 (V94F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2382628	NM_001126328.3(LNX1):c.275T>A (p.Ile92Asn)	LNX1 (I92N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383076	NM_001126328.3(LNX1):c.236G>A (p.Arg79His)	LNX1 (R79H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364312	NM_001126328.3(LNX1):c.164C>T (p.Pro55Leu)	LNX1 (P55L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2255855	NM_001126328.3(LNX1):c.134T>C (p.Leu45Pro)	LNX1 (L45P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119477	NM_001126328.3(LNX1):c.110A>G (p.Asp37Gly)	LNX1 (D37G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307910	NM_001126328.3(LNX1):c.37C>G (p.Leu13Val)	LNX1 (L13V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 52