NM_005138.3(SCO2):c.306C>T (p.Gly102=) AND SCO2-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jun 5, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003940998.2
Allele description [Variation Report for NM_005138.3(SCO2):c.306C>T (p.Gly102=)]
NM_005138.3(SCO2):c.306C>T (p.Gly102=)
Condition(s)
- Name:
- SCO2-related disorder
- Synonyms:
- SCO2-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Oct 13, 2024