C5551362[trait identifier] AND "Revvity Omics, Revvity"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2435263	NM_020719.3(PRR12):c.577C>G (p.Pro193Ala)	PRR12 (P193A)	Single nucleotide variant (missense variant)	Neuroocular syndrome	GUncertain significance
Select item 2689832	NM_020719.3(PRR12):c.2405T>A (p.Leu802His)	PRR12 (L802H)	Single nucleotide variant (missense variant)	Neuroocular syndrome	GUncertain significance
Select item 2432862	NM_020719.3(PRR12):c.3404C>A (p.Ser1135Ter)	PRR12 (S1135*)	Single nucleotide variant (nonsense)	Neuroocular syndrome	GLikely pathogenic

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