NM_000546.6(TP53):c.455C>T (p.Pro152Leu) AND not provided
- Germline classification:
- Pathogenic (1 submission)
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000583667.7
Allele description [Variation Report for NM_000546.6(TP53):c.455C>T (p.Pro152Leu)]
NM_000546.6(TP53):c.455C>T (p.Pro152Leu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024