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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2332184	NM_006433.5(GNLY):c.14C>T (p.Ala5Val)	GNLY (A5V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3100660	NM_006433.5(GNLY):c.89A>G (p.Asp30Gly)	GNLY (D15G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556804	NM_006433.5(GNLY):c.114T>G (p.Asp38Glu)	GNLY (D38E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2343590	NM_006433.5(GNLY):c.131C>T (p.Pro44Leu)	GNLY (P44L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347109	NM_006433.5(GNLY):c.158G>T (p.Gly53Val)	GNLY (G38V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3100659	NM_006433.5(GNLY):c.215T>C (p.Ile72Thr)	GNLY (I57T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556036	NM_006433.5(GNLY):c.290G>A (p.Arg97Lys)	GNLY (R82K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595816	NM_006433.5(GNLY):c.383C>T (p.Ala128Val)	GNLY (A113V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar