NM_000551.4(VHL):c.216C>A (p.Ser72=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 27, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000679021.5
Allele description [Variation Report for NM_000551.4(VHL):c.216C>A (p.Ser72=)]
NM_000551.4(VHL):c.216C>A (p.Ser72=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Mar 10, 2024