List of variants in gene PTEN reported as uncertain significance for Breast and/or ovarian cancer

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000314.8(PTEN):c.235G>A (p.Ala79Thr)	rs202004587	0.00011
NM_000314.8(PTEN):c.1061C>A (p.Pro354Gln)	rs375709098	0.00003
NM_000314.8(PTEN):c.210-9T>C	rs751744545	0.00001
NM_000314.8(PTEN):c.841C>G (p.Pro281Ala)	rs750705904	0.00001
NM_000314.8(PTEN):c.*10del	rs756681683
NM_000314.8(PTEN):c.253+7A>G	rs2132239067
NM_000314.8(PTEN):c.801+9T>C	rs1060503839
NM_000314.8(PTEN):c.802-5_802-3del	rs34003473
NM_000314.8(PTEN):c.838A>G (p.Ile280Val)	rs1474354667
NM_000314.8(PTEN):c.949G>A (p.Val317Ile)	rs876658630

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