"Fulgent Genetics, Fulgent Genetics"[submitter] AND "PRKD1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 732997	NM_002742.3(PRKD1):c.1441G>A (p.Ala481Thr)	PRKD1 (A481T +2 more)	Single nucleotide variant (missense variant)	Congenital heart defects and ectodermal dysplasia +1 more	GLikely benign
Select item 717322	NM_002742.3(PRKD1):c.265-5T>C	PRKD1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign