NM_001079668.3(NKX2-1):c.567G>T (p.Ala189=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000921371.3
Allele description [Variation Report for NM_001079668.3(NKX2-1):c.567G>T (p.Ala189=)]
NM_001079668.3(NKX2-1):c.567G>T (p.Ala189=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: CN517202
Assertion and evidence details
Last Updated: Aug 23, 2022