Showing 1 to 3 of 3 rows
See Report | Preferred Variant Title | Classification | Condition | Published Date | Version | Criteria Specification | Gene |
|---|---|---|---|---|---|---|---|
| View | NM_000546.5(TP53):c.847C>T (p.Arg283Cys) | Likely Benign | Li-Fraumeni syndrome | 2024-08-05 | 2.1 | ClinGen TP53 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for TP53 Version 2.0.0 | TP53 |
| View | NM_000546.5(TP53):c.847C>T (p.Arg283Cys) | Likely Benign | Li-Fraumeni syndrome | 2022-03-18 | 2.0 | - | TP53 |
| View | NM_000546.5(TP53):c.847C>T (p.Arg283Cys) | Uncertain Significance | Li-Fraumeni syndrome | 2020-01-24 | 1.0 | - | TP53 |
Showing 1 to 3 of 3 rows