NM_003239.5(TGFB3):c.1128T>C (p.Pro376=) AND Rienhoff syndrome
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 10, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003867790.1
Allele description [Variation Report for NM_003239.5(TGFB3):c.1128T>C (p.Pro376=)]
NM_003239.5(TGFB3):c.1128T>C (p.Pro376=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024