"Ambry Genetics"[submitter] AND "LINGO1"[gene] - ClinVar

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Items: 26

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2524804	NM_032808.7(LINGO1):c.1849A>T (p.Met617Leu)	LINGO1 (M611L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2348511	NM_032808.7(LINGO1):c.1816A>G (p.Ile606Val)	LINGO1 (I606V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2609637	NM_032808.7(LINGO1):c.1795C>G (p.Pro599Ala)	LINGO1 (P593A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475663	NM_032808.7(LINGO1):c.1711G>A (p.Val571Ile)	LINGO1 (V571I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2561115	NM_032808.7(LINGO1):c.1385G>A (p.Arg462Gln)	LINGO1 (R456Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2541586	NM_032808.7(LINGO1):c.1382C>A (p.Pro461His)	LINGO1 (P461H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2384834	NM_032808.7(LINGO1):c.1358C>T (p.Pro453Leu)	LINGO1 (P447L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2486553	NM_032808.7(LINGO1):c.1322C>T (p.Thr441Met)	LINGO1 (T435M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2378094	NM_032808.7(LINGO1):c.1274G>A (p.Arg425His)	LINGO1 (R425H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2601127	NM_032808.7(LINGO1):c.1184C>T (p.Thr395Met)	LINGO1 (T389M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2463269	NM_032808.7(LINGO1):c.1171C>T (p.Arg391Trp)	LINGO1 (R385W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2548259	NM_032808.7(LINGO1):c.1070C>T (p.Ser357Leu)	LINGO1 (S357L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2520337	NM_032808.7(LINGO1):c.997G>A (p.Gly333Ser)	LINGO1 (G327S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2620233	NM_032808.7(LINGO1):c.895A>G (p.Ile299Val)	LINGO1 (I293V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2515484	NM_032808.7(LINGO1):c.832G>A (p.Val278Met)	LINGO1 (V278M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2620232	NM_032808.7(LINGO1):c.821A>G (p.Asn274Ser)	LINGO1 (N274S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2297714	NM_032808.7(LINGO1):c.668G>A (p.Arg223Gln)	LINGO1 (R217Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2232748	NM_032808.7(LINGO1):c.484A>C (p.Met162Leu)	LINGO1 (M156L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2526293	NM_032808.7(LINGO1):c.461A>T (p.Lys154Met)	LINGO1 (K154M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2270158	NM_032808.7(LINGO1):c.452G>A (p.Ser151Asn)	LINGO1 (S145N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2291121	NM_032808.7(LINGO1):c.368C>T (p.Thr123Met)	LINGO1 (T117M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2475402	NM_032808.7(LINGO1):c.220C>T (p.Arg74Cys)	LINGO1 (R68C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2224324	NM_032808.7(LINGO1):c.146C>T (p.Ser49Phe)	LINGO1 (S49F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2218427	NM_032808.7(LINGO1):c.119C>T (p.Thr40Met)	LINGO1 (T40M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2616001	NM_032808.7(LINGO1):c.55C>T (p.Leu19Phe)	LINGO1 (L13F +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2605456	NM_032808.7(LINGO1):c.34G>A (p.Val12Met)	LINGO1 (V12M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 26