NM_001189.4(NKX3-2):c.987C>T (p.Ala329=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000889959.6
Allele description [Variation Report for NM_001189.4(NKX3-2):c.987C>T (p.Ala329=)]
NM_001189.4(NKX3-2):c.987C>T (p.Ala329=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024