"Genome Diagnostics Laboratory, Amsterdam University Medical Center"[s - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 717443	NM_001126049.2(KLLN):c.339_340del (p.Ala115fs)	KLLN, PTEN (A115fs)	Deletion (frameshift variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 824671	NM_000314.8(PTEN):c.41G>A (p.Arg14Lys)	PTEN (R187K +1 more)	Single nucleotide variant (missense variant +1 more)	Hereditary cancer-predisposing syndrome	GUncertain significance
Select item 231916	NM_000314.8(PTEN):c.103A>G (p.Met35Val)	PTEN (M35V +1 more)	Single nucleotide variant (missense variant +1 more)	PTEN hamartoma tumor syndrome	GLikely pathogenic FDA Recognized database
Select item 92813	NM_000314.8(PTEN):c.132C>T (p.Gly44=)	PTEN	Single nucleotide variant (synonymous variant +1 more)	PTEN hamartoma tumor syndrome	GLikely benign FDA Recognized database
Select item 7836	NM_000314.8(PTEN):c.633C>A (p.Cys211Ter)	PTEN (C211* +2 more)	Single nucleotide variant (nonsense)	PTEN-related condition +4 more	GPathogenic
Select item 229653	NM_000314.8(PTEN):c.802-3del	PTEN	Deletion (intron variant)	not specified +4 more	GBenign/Likely benign
Select item 92833	NM_000314.8(PTEN):c.802-4_802-3del	PTEN	Deletion (intron variant)	Breast and/or ovarian cancer +2 more	GBenign/Likely benign
Select item 7833	NM_000314.8(PTEN):c.1003C>T (p.Arg335Ter)	PTEN (R335* +2 more)	Single nucleotide variant (nonsense)	Malignant tumor of prostate +12 more	GPathogenic

ClinVar