NM_000030.3(AGXT):c.27C>A (p.Thr9=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 25, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000939994.8
Allele description [Variation Report for NM_000030.3(AGXT):c.27C>A (p.Thr9=)]
NM_000030.3(AGXT):c.27C>A (p.Thr9=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 7, 2024