NM_001103.4(ACTN2):c.1836C>T (p.Asp612=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 4, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003804091.1
Allele description [Variation Report for NM_001103.4(ACTN2):c.1836C>T (p.Asp612=)]
NM_001103.4(ACTN2):c.1836C>T (p.Asp612=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024