NM_000262.3(NAGA):c.418C>T (p.Gln140Ter) AND not provided
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Apr 17, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001508023.5
Allele description [Variation Report for NM_000262.3(NAGA):c.418C>T (p.Gln140Ter)]
NM_000262.3(NAGA):c.418C>T (p.Gln140Ter)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Dec 24, 2023