Showing 1 to 2 of 2 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000314.8(PTEN):c.892C>G (p.Gln298Glu) | Likely Benign | PTEN hamartoma tumor syndrome | 2023-10-19 | 2.0 | ClinGen PTEN Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for PTEN Version 3.0.0 | PTEN |
| View | NM_000314.6(PTEN):c.892C>G (p.Gln298Glu) | Uncertain Significance | PTEN hamartoma tumor syndrome | 2019-07-23 | 1.0 | - | PTEN |
Showing 1 to 2 of 2 rows