NM_152564.5(VPS13B):c.9645C>T (p.Leu3215=) AND not specified
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 13, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000194848.9
Allele description [Variation Report for NM_152564.5(VPS13B):c.9645C>T (p.Leu3215=)]
NM_152564.5(VPS13B):c.9645C>T (p.Leu3215=)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024