"Ambry Genetics"[submitter] AND "WARS1"[gene] - ClinVar

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Items: 34

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3189492	NM_004184.4(WARS1):c.1353G>T (p.Glu451Asp)	WARS1 (E410D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189491	NM_004184.4(WARS1):c.1346G>A (p.Arg449His)	WARS1 (R408H +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3332551	NM_004184.4(WARS1):c.1303A>G (p.Ile435Val)	WARS1 (I394V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2557277	NM_004184.4(WARS1):c.1297G>A (p.Ala433Thr)	WARS1 (A392T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2477804	NM_004184.4(WARS1):c.1235A>G (p.Lys412Arg)	WARS1 (K371R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3189489	NM_004184.4(WARS1):c.1231G>A (p.Asp411Asn)	WARS1 (D411N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189488	NM_004184.4(WARS1):c.1155G>T (p.Glu385Asp)	WARS1 (E344D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189487	NM_004184.4(WARS1):c.1063C>T (p.Pro355Ser)	WARS1 (P314S +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2611596	NM_004184.4(WARS1):c.1062C>A (p.Asp354Glu)	WARS1 (D313E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189486	NM_004184.4(WARS1):c.1058G>C (p.Ser353Thr)	WARS1 (S312T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189508	NM_004184.4(WARS1):c.967G>A (p.Val323Ile)	WARS1 (V282I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189507	NM_004184.4(WARS1):c.893G>A (p.Arg298Gln)	WARS1 (R298Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2672568	NM_004184.4(WARS1):c.817G>A (p.Asp273Asn)	WARS1 (D232N +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3189506	NM_004184.4(WARS1):c.772G>A (p.Val258Ile)	WARS1 (V217I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2592873	NM_004184.4(WARS1):c.700A>G (p.Ile234Val)	WARS1 (I234V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 3189504	NM_004184.4(WARS1):c.677G>C (p.Gly226Ala)	WARS1 (G185A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189503	NM_004184.4(WARS1):c.523A>G (p.Ile175Val)	WARS1 (I134V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189502	NM_004184.4(WARS1):c.485G>A (p.Arg162Gln)	WARS1 (R162Q +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2455963	NM_004184.4(WARS1):c.446C>A (p.Ala149Asp)	WARS1 (A108D +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189501	NM_004184.4(WARS1):c.440T>G (p.Leu147Arg)	WARS1 (L106R +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189500	NM_004184.4(WARS1):c.439C>G (p.Leu147Val)	WARS1 (L106V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189499	NM_004184.4(WARS1):c.407T>C (p.Ile136Thr)	WARS1 (I136T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2485684	NM_004184.4(WARS1):c.397C>T (p.Arg133Cys)	WARS1 (R133C +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 3189498	NM_004184.4(WARS1):c.359T>C (p.Ile120Thr)	WARS1 (I79T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2513545	NM_004184.4(WARS1):c.339C>A (p.Asp113Glu)	WARS1 (D72E +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2608632	NM_004184.4(WARS1):c.316C>T (p.Arg106Trp)	WARS1 (R106W +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189497	NM_004184.4(WARS1):c.301G>A (p.Asp101Asn)	WARS1 (D60N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189496	NM_004184.4(WARS1):c.281G>A (p.Ser94Asn)	WARS1 (S53N +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189495	NM_004184.4(WARS1):c.236A>T (p.Glu79Val)	WARS1 (E38V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 3189494	NM_004184.4(WARS1):c.160G>A (p.Ala54Thr)	WARS1 (A13T +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3189490	NM_004184.4(WARS1):c.130G>C (p.Val44Leu)	WARS1 (V3L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 3189505	NM_004184.4(WARS1):c.67G>A (p.Val23Ile)	WARS1 (V23I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3332550	NM_004184.4(WARS1):c.50C>T (p.Ala17Val)	WARS1 (A17V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 3332549	NM_004184.4(WARS1):c.49G>A (p.Ala17Thr)	WARS1 (A17T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance

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Items: 34