NM_002661.5(PLCG2):c.784C>G (p.Leu262Val) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001532287.19
Allele description [Variation Report for NM_002661.5(PLCG2):c.784C>G (p.Leu262Val)]
NM_002661.5(PLCG2):c.784C>G (p.Leu262Val)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Oct 8, 2024