NM_032520.5(GNPTG):c.744T>G (p.Ala248=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 25, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000921284.6
Allele description [Variation Report for NM_032520.5(GNPTG):c.744T>G (p.Ala248=)]
NM_032520.5(GNPTG):c.744T>G (p.Ala248=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024