NM_006218.4(PIK3CA):c.291C>T (p.Pro97=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002434195.9
Allele description [Variation Report for NM_006218.4(PIK3CA):c.291C>T (p.Pro97=)]
NM_006218.4(PIK3CA):c.291C>T (p.Pro97=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 1, 2024