"NARS1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2628986	NM_004539.4(NARS1):c.1561G>C (p.Glu521Gln)	NARS1 (E521Q)	Single nucleotide variant (missense variant)	NARS1-related condition	GUncertain significance
Select item 2524841	NM_004539.4(NARS1):c.1189A>G (p.Ile397Val)	NARS1 (I397V)	Single nucleotide variant (missense variant)	NARS1-related condition +2 more	GLikely benign
Select item 2631445	NM_004539.4(NARS1):c.925C>T (p.Pro309Ser)	NARS1 (P309S)	Single nucleotide variant (missense variant)	NARS1-related condition	GUncertain significance
Select item 2633360	NM_004539.4(NARS1):c.535G>A (p.Val179Ile)	NARS1 (V179I)	Single nucleotide variant (missense variant)	NARS1-related condition	GUncertain significance
Select item 2635992	NM_004539.4(NARS1):c.412C>T (p.Arg138Cys)	NARS1 (R138C)	Single nucleotide variant (missense variant)	NARS1-related condition	GUncertain significance
Select item 2634674	NM_004539.4(NARS1):c.311A>G (p.Lys104Arg)	NARS1 (K104R)	Single nucleotide variant (missense variant)	NARS1-related condition	GUncertain significance
Select item 3043011	NM_004539.4(NARS1):c.251_252del (p.Glu84fs)	NARS1 (E84fs)	Microsatellite (frameshift variant)	NARS1-related condition	GPathogenic

ClinVar