NM_001330677.2(TBX15):c.676T>C (p.Leu226=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jul 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002182574.5
Allele description [Variation Report for NM_001330677.2(TBX15):c.676T>C (p.Leu226=)]
NM_001330677.2(TBX15):c.676T>C (p.Leu226=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 20, 2024