"DBGen Ocular Genomics"[submitter] AND "NYX"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1213864	NM_001378477.3(NYX):c.371_372dup (p.Thr125fs)	NYX (T125fs)	Microsatellite (frameshift variant)	Congenital stationary night blindness 1A	GUncertain significance
Select item 1213862	NM_001378477.3(NYX):c.689dup (p.Leu231fs)	NYX (L231fs)	Duplication (frameshift variant)	Retinal dystrophy	GPathogenic
Select item 1213863	NM_001378477.3(NYX):c.704A>G (p.Asn235Ser)	NYX (N235S)	Single nucleotide variant (missense variant)	Retinitis pigmentosa	GUncertain significance

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