NM_145239.3(PRRT2):c.751T>C (p.Leu251=) AND not specified
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jul 15, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000153784.7
Allele description [Variation Report for NM_145239.3(PRRT2):c.751T>C (p.Leu251=)]
NM_145239.3(PRRT2):c.751T>C (p.Leu251=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 29, 2024