C1959582[trait identifier] AND "Seattle Children's Hospital Molecular - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 427613	NM_000314.8(PTEN):c.165-1G>C	PTEN	Single nucleotide variant (splice acceptor variant +1 more)	PTEN hamartoma tumor syndrome	GPathogenicFDA Recognized database
Select item 7819	NM_000314.8(PTEN):c.388C>T (p.Arg130Ter)	PTEN (R130* +1 more)	Single nucleotide variant (nonsense +1 more)	Malignant tumor of prostate +9 more	GPathogenic OOncogenic
Select item 92822	NM_000314.8(PTEN):c.395G>A (p.Gly132Asp)	PTEN (G132D +1 more)	Single nucleotide variant (missense variant +1 more)	PTEN hamartoma tumor syndrome	GPathogenicFDA Recognized database
Select item 1067498	NM_000314.8(PTEN):c.493G>C (p.Gly165Arg)	PTEN (G165R +1 more)	Single nucleotide variant (missense variant +1 more)	Cowden syndrome 1 +2 more	GPathogenic/Likely pathogenic
Select item 481172	NM_000314.8(PTEN):c.1008C>G (p.Tyr336Ter)	PTEN (Y336* +2 more)	Single nucleotide variant (nonsense)	Hereditary cancer-predisposing syndrome +2 more	GPathogenic
Select item 143020	NM_000314.8(PTEN):c.1061C>A (p.Pro354Gln)	PTEN (P354Q +2 more)	Single nucleotide variant (missense variant)	PTEN hamartoma tumor syndrome	GLikely benignFDA Recognized database

ClinVar