NM_152594.3(SPRED1):c.872A>T (p.Asp291Val) AND Legius syndrome
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 9, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003497522.1
Allele description [Variation Report for NM_152594.3(SPRED1):c.872A>T (p.Asp291Val)]
NM_152594.3(SPRED1):c.872A>T (p.Asp291Val)
Condition(s)
Assertion and evidence details
Last Updated: Sep 1, 2024