C3551915[trait identifier] AND "Genetics and Molecular Pathology, SA P - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 7819	NM_000314.8(PTEN):c.388C>T (p.Arg130Ter)	PTEN (R130* +1 more)	Single nucleotide variant (nonsense +1 more)	PTEN-related condition +8 more	GPathogenic
Select item 127695	NM_000314.8(PTEN):c.892C>G (p.Gln298Glu)	PTEN (Q298E +2 more)	Single nucleotide variant (missense variant)	PTEN hamartoma tumor syndrome	GLikely benign FDA Recognized database
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
Select item 1803278	NM_003079.5(SMARCE1):c.683_685delinsT (p.Lys228fs)	SMARCE1 (K228fs)	Indel (frameshift variant)	Familial meningioma	GLikely pathogenic
Select item 2664741	NM_003079.5(SMARCE1):c.587del (p.Phe196fs)	SMARCE1 (F196fs)	Deletion (frameshift variant)	Familial meningioma	GPathogenic
Select item 2664726	NM_003079.5(SMARCE1):c.585_586delinsA (p.Phe196fs)	SMARCE1 (F196fs)	Indel (frameshift variant)	Familial meningioma	GLikely pathogenic

ClinVar