ClinVar (all) for Orgtrack (Select 509734) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3362882	NM_001304360.2(CFAP74):c.2452C>T (p.Arg818Trp)	CFAP74 (R818W)	Single nucleotide variant (missense variant)	CFAP74-related disorder	GLikely pathogenic
Select item 3362881	NM_001304360.2(CFAP74):c.3044T>C (p.Val1015Ala)	CFAP74 (V1015A)	Single nucleotide variant (missense variant)	CFAP74-related disorder	GLikely pathogenic