NM_004573.3(PLCB2):c.1489T>C (p.Trp497Arg) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 3, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004511751.1
Allele description [Variation Report for NM_004573.3(PLCB2):c.1489T>C (p.Trp497Arg)]
NM_004573.3(PLCB2):c.1489T>C (p.Trp497Arg)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: May 7, 2024