"Ambry Genetics"[submitter] AND "VSIG10L-AS1"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2257733	NM_001163922.3(VSIG10L):c.1345G>C (p.Ala449Pro)	LOC130065026, VSIG10L +1 more (A449P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2245095	NM_001163922.3(VSIG10L):c.1283G>A (p.Cys428Tyr)	VSIG10L, VSIG10L-AS1 (C428Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2375613	NM_001163922.3(VSIG10L):c.1274C>T (p.Thr425Ile)	VSIG10L, VSIG10L-AS1 (T425I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314940	NM_001163922.3(VSIG10L):c.1258G>A (p.Ala420Thr)	VSIG10L, VSIG10L-AS1 (A420T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2355628	NM_001163922.3(VSIG10L):c.1216G>C (p.Val406Leu)	VSIG10L, VSIG10L-AS1 (V406L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2328918	NM_001163922.3(VSIG10L):c.1190A>G (p.Tyr397Cys)	VSIG10L, VSIG10L-AS1 (Y397C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2523921	NM_001163922.3(VSIG10L):c.1147C>T (p.Pro383Ser)	VSIG10L, VSIG10L-AS1 (P383S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2362346	NM_001163922.3(VSIG10L):c.1139T>G (p.Val380Gly)	VSIG10L, VSIG10L-AS1 (V380G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2510366	NM_001163922.3(VSIG10L):c.1088T>G (p.Leu363Arg)	VSIG10L, VSIG10L-AS1 (L363R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2474778	NM_001163922.3(VSIG10L):c.1083C>A (p.Asp361Glu)	VSIG10L, VSIG10L-AS1 (D361E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2458896	NM_001163922.3(VSIG10L):c.980G>C (p.Trp327Ser)	VSIG10L, VSIG10L-AS1 (W327S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2404455	NM_001163922.3(VSIG10L):c.947G>T (p.Gly316Val)	VSIG10L, VSIG10L-AS1 (G316V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2314285	NM_001163922.3(VSIG10L):c.887G>T (p.Gly296Val)	VSIG10L, VSIG10L-AS1 (G296V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2239914	NM_001163922.3(VSIG10L):c.614C>T (p.Thr205Ile)	VSIG10L, VSIG10L-AS1 (T205I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2553959	NM_001163922.3(VSIG10L):c.503T>G (p.Met168Arg)	VSIG10L, VSIG10L-AS1 (M168R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2213316	NM_001163922.3(VSIG10L):c.497A>T (p.Asp166Val)	VSIG10L, VSIG10L-AS1 (D166V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2564780	NM_001163922.3(VSIG10L):c.494C>T (p.Pro165Leu)	VSIG10L, VSIG10L-AS1 (P165L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2610440	NM_001163922.3(VSIG10L):c.481T>G (p.Ser161Ala)	VSIG10L, VSIG10L-AS1 (S161A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2488613	NM_001163922.3(VSIG10L):c.410C>A (p.Thr137Asn)	VSIG10L, VSIG10L-AS1 (T137N)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2331572	NM_001163922.3(VSIG10L):c.404C>G (p.Ser135Cys)	VSIG10L-AS1, VSIG10L (S135C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2336804	NM_001163922.3(VSIG10L):c.394C>T (p.Pro132Ser)	VSIG10L, VSIG10L-AS1 (P132S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2359378	NM_001163922.3(VSIG10L):c.317C>T (p.Pro106Leu)	VSIG10L, VSIG10L-AS1 (P106L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2600271	NM_001163922.3(VSIG10L):c.137A>T (p.Gln46Leu)	VSIG10L, VSIG10L-AS1 (Q46L)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2481352	NM_001163922.3(VSIG10L):c.85C>G (p.Gln29Glu)	VSIG10L, VSIG10L-AS1 (Q29E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2350138	NM_001163922.3(VSIG10L):c.6C>A (p.Asp2Glu)	VSIG10L, VSIG10L-AS1 (D2E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Items: 25