NM_018100.4(EFHC1):c.961T>C (p.Leu321=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 25, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003771426.2
Allele description [Variation Report for NM_018100.4(EFHC1):c.961T>C (p.Leu321=)]
NM_018100.4(EFHC1):c.961T>C (p.Leu321=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024