"PreventionGenetics, part of Exact Sciences"[submitter] AND "GNAT1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1624682	NM_144499.3(GNAT1):c.45G>A (p.Leu15=)	GNAT1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 933848	NM_144499.3(GNAT1):c.292-3C>T	GNAT1	Single nucleotide variant (intron variant)	GNAT1-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 346049	NM_144499.3(GNAT1):c.294C>T (p.Asp98=)	GNAT1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 903401	NM_144499.3(GNAT1):c.411G>A (p.Glu137=)	GNAT1	Single nucleotide variant (synonymous variant)	Congenital stationary night blindness autosomal dominant 3 +2 more	GBenign/Likely benign
Select item 346051	NM_144499.3(GNAT1):c.830C>T (p.Ala277Val)	GNAT1 (A277V)	Single nucleotide variant (missense variant)	GNAT1-related disorder +1 more	GUncertain significance
Select item 346052	NM_144499.3(GNAT1):c.876C>T (p.Tyr292=)	GNAT1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 346053	NM_144499.3(GNAT1):c.882C>T (p.Asp294=)	GNAT1	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 346055	NM_144499.3(GNAT1):c.939G>A (p.Lys313=)	GNAT1	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign

ClinVar