NM_001614.5(ACTG1):c.657C>T (p.Val219=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 28, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000954546.6
Allele description [Variation Report for NM_001614.5(ACTG1):c.657C>T (p.Val219=)]
NM_001614.5(ACTG1):c.657C>T (p.Val219=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024