NM_000551.4(VHL):c.222C>T (p.Val74=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 31, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001450899.6
Allele description [Variation Report for NM_000551.4(VHL):c.222C>T (p.Val74=)]
NM_000551.4(VHL):c.222C>T (p.Val74=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024