NM_152564.5(VPS13B):c.11071G>A (p.Ala3691Thr) AND Cohen syndrome
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000361059.27
Allele description [Variation Report for NM_152564.5(VPS13B):c.11071G>A (p.Ala3691Thr)]
NM_152564.5(VPS13B):c.11071G>A (p.Ala3691Thr)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024