NM_001136271.3(NKX2-6):c.867C>T (p.Gly289=) AND Conotruncal heart malformations
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 22, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000642306.5
Allele description [Variation Report for NM_001136271.3(NKX2-6):c.867C>T (p.Gly289=)]
NM_001136271.3(NKX2-6):c.867C>T (p.Gly289=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024