"Pars Genome Lab"[submitter] AND "CACNA1F"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2503479	NM_001256789.3(CACNA1F):c.982A>G (p.Thr328Ala)	CACNA1F (T263A +1 more)	Single nucleotide variant (missense variant)	X-linked cone-rod dystrophy 3	GLikely benign
Select item 2503472	NM_001256789.3(CACNA1F):c.25+1G>A	CACNA1F (G9D)	Single nucleotide variant (missense variant +1 more)	X-linked cone-rod dystrophy 3	GLikely benign