NM_001101.5(ACTB):c.1116C>T (p.Arg372=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003423546.5
Allele description [Variation Report for NM_001101.5(ACTB):c.1116C>T (p.Arg372=)]
NM_001101.5(ACTB):c.1116C>T (p.Arg372=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 12, 2024