NM_003722.5(TP63):c.1587C>T (p.Leu529=) AND TP63-Related Spectrum Disorders
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 19, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000357046.15
Allele description [Variation Report for NM_003722.5(TP63):c.1587C>T (p.Leu529=)]
NM_003722.5(TP63):c.1587C>T (p.Leu529=)
Condition(s)
- Name:
- TP63-Related Spectrum Disorders
- Identifiers:
- MedGen: CN239305
Assertion and evidence details
Last Updated: May 12, 2024