NM_001029883.3(PCARE):c.2889C>T (p.Ser963=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 29, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001516842.6
Allele description [Variation Report for NM_001029883.3(PCARE):c.2889C>T (p.Ser963=)]
NM_001029883.3(PCARE):c.2889C>T (p.Ser963=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 23, 2024