NM_032520.5(GNPTG):c.837G>A (p.Leu279=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001243901.3
Allele description [Variation Report for NM_032520.5(GNPTG):c.837G>A (p.Leu279=)]
NM_032520.5(GNPTG):c.837G>A (p.Leu279=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024