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

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2474496	NM_006178.4(NSF):c.1031C>T (p.Thr344Met)	LRRC37A2, NSF (T344M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2528002	NM_006178.4(NSF):c.1039C>T (p.His347Tyr)	LRRC37A2, NSF (H347Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2308915	NM_006178.4(NSF):c.1246G>A (p.Gly416Arg)	LRRC37A2, NSF (G416R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3301145	NM_006178.4(NSF):c.1615G>A (p.Val539Met)	LRRC37A2, NSF (V539M)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2329962	NM_006178.4(NSF):c.2009T>C (p.Ile670Thr)	LRRC37A2, NSF (I670T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2318210	NM_006178.4(NSF):c.2071C>T (p.Arg691Cys)	LRRC37A2, NSF (R691C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3202345	NM_006178.4(NSF):c.2074A>G (p.Thr692Ala)	LRRC37A2, NSF (T692A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar