List of variants in gene PTEN reported as uncertain significance by Department of Pathology and Laboratory Medicine, Sinai Health System

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.892C>G (p.Gln298Glu)	rs371387815	0.00009
NM_000314.8(PTEN):c.1061C>A (p.Pro354Gln)	rs375709098	0.00003
NM_000314.8(PTEN):c.114T>G (p.Pro38=)	rs748040144	0.00001
NM_000314.8(PTEN):c.-6C>A	rs1554890322
NM_000314.8(PTEN):c.1083T>C (p.Ser361=)	rs2132289564
NM_000314.8(PTEN):c.210-7_210-3del	rs587780544
NM_000314.8(PTEN):c.218A>G (p.Glu73Gly)	rs2132238743

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