"Eurofins Ntd Llc (ga)"[submitter] AND "PRKN"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 283504	NM_004562.3(PRKN):c.1310C>T (p.Pro437Leu)	PRKN (P437L +2 more)	Single nucleotide variant (missense variant)	Autosomal recessive juvenile Parkinson disease 2 +5 more	GConflicting classifications of pathogenicity
Select item 41222	NM_004562.3(PRKN):c.1180G>A (p.Asp394Asn)	PRKN (D394N +2 more)	Single nucleotide variant (missense variant)	Ovarian neoplasm +4 more	GBenign/Likely benign
Select item 41221	NM_004562.3(PRKN):c.1138G>C (p.Val380Leu)	PRKN (V380L +2 more)	Single nucleotide variant (missense variant)	not specified +4 more	GBenign
Select item 199099	NM_004562.3(PRKN):c.1017G>A (p.Ala339=)	PRKN	Single nucleotide variant (synonymous variant)	not specified +1 more	GBenign
Select item 281504	NM_004562.3(PRKN):c.1000C>T (p.Arg334Cys)	PRKN (R334C +2 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 415531	NM_004562.3(PRKN):c.574A>C (p.Met192Leu)	PRKN (M192L)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GBenign
Select item 289182	NM_004562.3(PRKN):c.48G>A (p.Glu16=)	PRKN	Single nucleotide variant (synonymous variant)	not specified +2 more	GConflicting classifications of pathogenicity

ClinVar