NM_001614.5(ACTG1):c.877C>T (p.Leu293=) AND multiple conditions
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 8, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000873651.9
Allele description [Variation Report for NM_001614.5(ACTG1):c.877C>T (p.Leu293=)]
NM_001614.5(ACTG1):c.877C>T (p.Leu293=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024