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See Report
Preferred Variant Title
Classification
Condition
Published Date
Version
Criteria Specification
Gene
View NM_001126112.2(TP53):c.509C>T (p.Thr170Met)
Likely Benign
Li-Fraumeni syndrome2025-02-07
2.0
ClinGen TP53 Expert Panel Specifications to the ACMG/AMP Variant Interpretation Guidelines for TP53 Version 2.2.0TP53
View NM_001126112.2(TP53):c.509C>T (p.Thr170Met)
Likely Benign
Li-Fraumeni syndrome 12021-06-16
1.0
-TP53
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