NM_181675.4(PPP2R2B):c.803C>T (p.Pro268Leu) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 26, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004154597.1
Allele description [Variation Report for NM_181675.4(PPP2R2B):c.803C>T (p.Pro268Leu)]
NM_181675.4(PPP2R2B):c.803C>T (p.Pro268Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Jul 15, 2024