NM_207351.5(PRRT3):c.1190C>T (p.Pro397Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 6, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004097985.1
Allele description [Variation Report for NM_207351.5(PRRT3):c.1190C>T (p.Pro397Leu)]
NM_207351.5(PRRT3):c.1190C>T (p.Pro397Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 26, 2024