"Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, E - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 518334	NM_003690.5(PRKRA):c.861C>T (p.Ser287=)	CHROMR, PRKRA	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 332623	NM_003690.5(PRKRA):c.685C>T (p.Leu229=)	CHROMR, PRKRA	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign
Select item 522281	NM_001139517.1(PRKRA):c.27_28ins57 (p.?)	PRKRA	Insertion	Dystonia 16	GBenign

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