"PreventionGenetics, part of Exact Sciences"[submitter] AND "NAT2"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 726	NM_000015.3(NAT2):c.191G>A (p.Arg64Gln)	NAT2 (R64Q)	Single nucleotide variant (missense variant)	NAT2-related disorder	GLikely benign
Select item 3034766	NM_000015.3(NAT2):c.246C>T (p.Ile82=)	NAT2	Single nucleotide variant (synonymous variant)	NAT2-related disorder	GLikely benign
Select item 3060182	NM_000015.3(NAT2):c.282C>T (p.Tyr94=)	NAT2	Single nucleotide variant (synonymous variant)	NAT2-related disorder	GBenign
Select item 723	NM_000015.2(NAT2):c.341T>C (p.Ile114Thr)	NAT2 (I114T)	Single nucleotide variant (missense variant)	NAT2-related disorder	GBenign
Select item 3044340	NM_000015.3(NAT2):c.387C>T (p.Ser129=)	NAT2	Single nucleotide variant (synonymous variant)	NAT2-related disorder	GLikely benign
Select item 3060382	NM_000015.3(NAT2):c.481C>T (p.Leu161=)	NAT2	Single nucleotide variant (synonymous variant)	NAT2-related disorder	GBenign
Select item 3046292	NM_000015.3(NAT2):c.504G>A (p.Gln168=)	NAT2	Single nucleotide variant (synonymous variant)	NAT2-related disorder	GLikely benign
Select item 722	NM_000015.3(NAT2):c.590G>A (p.Arg197Gln)	NAT2 (R197Q)	Single nucleotide variant (missense variant)	NAT2-related disorder	GBenign
Select item 3059207	NM_000015.3(NAT2):c.803G>A (p.Arg268Lys)	NAT2 (R268K)	Single nucleotide variant (missense variant)	NAT2-related disorder	GLikely benign

ClinVar