NM_006218.4(PIK3CA):c.186T>C (p.Leu62=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002415090.2
Allele description [Variation Report for NM_006218.4(PIK3CA):c.186T>C (p.Leu62=)]
NM_006218.4(PIK3CA):c.186T>C (p.Leu62=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
hcfc1b [Poecilia formosa]
hcfc1b [Poecilia formosa]Gene ID:103130748Gene
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Last Updated: May 1, 2024