"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "SUOX"[gene - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 309820	NM_000456.2(SUOX):c.-326A>T	SUOX	Single nucleotide variant	not provided +1 more	GLikely benign
Select item 998643	NM_001032386.2(SUOX):c.545G>A (p.Arg182His)	SUOX (R182H)	Single nucleotide variant (missense variant)	Sulfite oxidase deficiency +1 more	GUncertain significance
Select item 309837	NM_001032386.2(SUOX):c.629C>T (p.Pro210Leu)	SUOX (P210L)	Single nucleotide variant (missense variant)	Sulfite oxidase deficiency +2 more	GBenign/Likely benign
Select item 872169	NM_001032386.2(SUOX):c.1243G>A (p.Asp415Asn)	SUOX (D415N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 789616	NM_001032386.2(SUOX):c.1297C>T (p.Arg433Trp)	SUOX (R433W)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely benign
Select item 1675502	NM_001032386.2(SUOX):c.1556C>G (p.Pro519Arg)	SUOX (P519R)	Single nucleotide variant (missense variant)	not provided	GLikely pathogenic

ClinVar