NM_000543.5(SMPD1):c.1773T>A (p.Arg591=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 31, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003808001.1
Allele description [Variation Report for NM_000543.5(SMPD1):c.1773T>A (p.Arg591=)]
NM_000543.5(SMPD1):c.1773T>A (p.Arg591=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024