"Ambry Genetics"[submitter] AND "LINGO2"[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2480872	NM_001258282.3(LINGO2):c.1748C>T (p.Pro583Leu)	LINGO2 (P583L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319865	NM_001258282.3(LINGO2):c.1730T>C (p.Ile577Thr)	LINGO2 (I577T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379705	NM_001258282.3(LINGO2):c.1724A>G (p.Asn575Ser)	LINGO2 (N575S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350973	NM_001258282.3(LINGO2):c.1594A>G (p.Asn532Asp)	LINGO2 (N532D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118997	NM_001258282.3(LINGO2):c.1533G>A (p.Ala511=)	LINGO2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2591222	NM_001258282.3(LINGO2):c.1438A>G (p.Met480Val)	LINGO2 (M480V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118996	NM_001258282.3(LINGO2):c.1349G>C (p.Arg450Pro)	LINGO2 (R450P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118995	NM_001258282.3(LINGO2):c.1166G>A (p.Arg389His)	LINGO2 (R389H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2395050	NM_001258282.3(LINGO2):c.1097T>C (p.Ile366Thr)	LINGO2 (I366T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611443	NM_001258282.3(LINGO2):c.1004C>G (p.Thr335Ser)	LINGO2 (T335S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612752	NM_001258282.3(LINGO2):c.908A>G (p.His303Arg)	LINGO2 (H303R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119001	NM_001258282.3(LINGO2):c.881C>G (p.Ser294Cys)	LINGO2 (S294C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242436	NM_001258282.3(LINGO2):c.642C>G (p.Asn214Lys)	LINGO2 (N214K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312431	NM_001258282.3(LINGO2):c.486C>A (p.Asp162Glu)	LINGO2 (D162E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2599115	NM_001258282.3(LINGO2):c.427A>C (p.Ile143Leu)	LINGO2 (I143L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297188	NM_001258282.3(LINGO2):c.377C>T (p.Thr126Met)	LINGO2 (T126M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2322630	NM_001258282.3(LINGO2):c.358G>C (p.Val120Leu)	LINGO2 (V120L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491459	NM_001258282.3(LINGO2):c.332G>A (p.Arg111His)	LINGO2 (R111H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207213	NM_001258282.3(LINGO2):c.308A>G (p.Asn103Ser)	LINGO2 (N103S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118999	NM_001258282.3(LINGO2):c.284A>G (p.Asn95Ser)	LINGO2 (N95S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118998	NM_001258282.3(LINGO2):c.176C>T (p.Thr59Ile)	LINGO2 (T59I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3119000	NM_001258282.3(LINGO2):c.53T>G (p.Val18Gly)	LINGO2 (V18G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548984	NM_001258282.3(LINGO2):c.14C>T (p.Ala5Val)	LINGO2 (A5V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 23