NM_003239.5(TGFB3):c.872C>T (p.Pro291Leu) AND multiple conditions
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002496780.8
Allele description [Variation Report for NM_003239.5(TGFB3):c.872C>T (p.Pro291Leu)]
NM_003239.5(TGFB3):c.872C>T (p.Pro291Leu)
Condition(s)
Assertion and evidence details
Last Updated: May 26, 2024