NM_000543.5(SMPD1):c.1467C>T (p.Thr489=) AND multiple conditions
- Germline classification:
- Likely 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:
- RCV002104433.5
Allele description [Variation Report for NM_000543.5(SMPD1):c.1467C>T (p.Thr489=)]
NM_000543.5(SMPD1):c.1467C>T (p.Thr489=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024