NM_003239.5(TGFB3):c.1213GTG[1] (p.Val406del) AND Rienhoff syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 11, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002890847.2
Allele description [Variation Report for NM_003239.5(TGFB3):c.1213GTG[1] (p.Val406del)]
NM_003239.5(TGFB3):c.1213GTG[1] (p.Val406del)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024