C1854369[trait identifier] AND "Centogene AG - the Rare Disease Compan - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1333855	NM_002739.5(PRKCG):c.220C>T (p.His74Tyr)	PRKCG (H74Y)	Single nucleotide variant (missense variant)	not provided +1 more	GLikely pathogenic
Select item 1333856	NM_002739.5(PRKCG):c.686+300C>G	PRKCG	Single nucleotide variant (intron variant)	Spinocerebellar ataxia type 14	GUncertain significance
Select item 518306	NM_002739.5(PRKCG):c.1747G>A (p.Val583Met)	PRKCG (V583M)	Single nucleotide variant (missense variant)	Spinocerebellar ataxia type 14 +1 more	GConflicting classifications of pathogenicity

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