NM_001101.5(ACTB):c.1125C>T (p.Phe375=) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Mar 20, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002285893.2
Allele description [Variation Report for NM_001101.5(ACTB):c.1125C>T (p.Phe375=)]
NM_001101.5(ACTB):c.1125C>T (p.Phe375=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Apr 15, 2023