Related gene-specific medical variations for Gene (Select 6821) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1325157	NM_001032386.2(SUOX):c.528T>A (p.Tyr176Ter)	SUOX (Y176*)	Single nucleotide variant (nonsense)	Sulfite oxidase deficiency	GLikely pathogenic
Select item 930742	NM_001032386.2(SUOX):c.599C>T (p.Pro200Leu)	SUOX (P200L)	Single nucleotide variant (missense variant)	Sulfite oxidase deficiency	GLikely pathogenic
Select item 3822	S370Y	SUOX	Single nucleotide variant	Sulfite oxidase deficiency	GPathogenic

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