"PreventionGenetics, part of Exact Sciences"[submitter] AND "WARS1"[ge - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3039971	NM_004184.4(WARS1):c.1398G>T (p.Leu466=)	WARS1	Single nucleotide variant (synonymous variant)	WARS1-related disorder	GLikely benign
Select item 1879286	NM_004184.4(WARS1):c.1230C>T (p.Asp410=)	WARS1	Single nucleotide variant (synonymous variant)	WARS1-related disorder +1 more	GBenign/Likely benign
Select item 2570889	NM_004184.4(WARS1):c.1038C>G (p.Ala346=)	WARS1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1265241	NM_004184.4(WARS1):c.1003C>T (p.Leu335=)	WARS1	Single nucleotide variant (synonymous variant)	Neuronopathy, distal hereditary motor, type 9 +2 more	GBenign
Select item 3036551	NM_004184.4(WARS1):c.875C>T (p.Ser292Leu)	WARS1 (S251L +1 more)	Single nucleotide variant (missense variant)	WARS1-related disorder	GUncertain significance
Select item 1178170	NM_004184.4(WARS1):c.826+6A>G	WARS1	Single nucleotide variant (intron variant)	WARS1-related disorder +2 more	GBenign
Select item 3029385	NM_004184.4(WARS1):c.699C>G (p.Phe233Leu)	WARS1 (F192L +1 more)	Single nucleotide variant (missense variant)	WARS1-related disorder	GUncertain significance
Select item 2644531	NM_004184.4(WARS1):c.669C>T (p.Ile223=)	WARS1	Single nucleotide variant (synonymous variant)	WARS1-related disorder +1 more	GLikely benign
Select item 783049	NM_004184.4(WARS1):c.25C>G (p.Leu9Val)	WARS1 (L9V)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign