NM_003722.5(TP63):c.996G>A (p.Gly332=) AND TP63-Related Spectrum Disorders
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003855080.2
Allele description [Variation Report for NM_003722.5(TP63):c.996G>A (p.Gly332=)]
NM_003722.5(TP63):c.996G>A (p.Gly332=)
Condition(s)
- Name:
- TP63-Related Spectrum Disorders
- Identifiers:
- MedGen: CN239305
Assertion and evidence details
Last Updated: Sep 29, 2024