NM_001136139.4(TCF3):c.1765C>T (p.Leu589=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Jan 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002126261.11
Allele description
NM_001136139.4(TCF3):c.1765C>T (p.Leu589=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 17, 2024