NM_005876.5(SPEG):c.1149C>T (p.Arg383=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002159381.6
Allele description [Variation Report for NM_005876.5(SPEG):c.1149C>T (p.Arg383=)]
NM_005876.5(SPEG):c.1149C>T (p.Arg383=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024