NM_006218.4(PIK3CA):c.1602T>C (p.Ile534=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 4, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002405065.2
Allele description [Variation Report for NM_006218.4(PIK3CA):c.1602T>C (p.Ile534=)]
NM_006218.4(PIK3CA):c.1602T>C (p.Ile534=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
cytochrome b, partial (mitochondrion) [Hypotaenidia sylvestris]
cytochrome b, partial (mitochondrion) [Hypotaenidia sylvestris]gi|459377106|gb|AGG58757.1|Protein
-
Gene rich cluster, C10 gene [Mus musculus]
Gene rich cluster, C10 gene [Mus musculus]gi|13543002|gb|AAH05683.1|Protein
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Last Updated: Sep 29, 2024