"Laboratory of Prof. Karen Avraham, Tel Aviv University"[submitter] AN - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3250394	NM_001191057.4(PDE1C):c.2061C>A (p.Tyr687Ter)	PDE1C (Y687* +1 more)	Single nucleotide variant (nonsense)	Hearing loss, autosomal dominant 74	GLikely pathogenic
Select item 3250393	NM_001191057.4(PDE1C):c.1900C>T (p.Gln634Ter)	PDE1C (Q634* +1 more)	Single nucleotide variant (nonsense)	Hearing loss, autosomal dominant 74	GLikely pathogenic