NM_000551.4(VHL):c.75T>C (p.Pro25=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Jan 12, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000540018.10
Allele description [Variation Report for NM_000551.4(VHL):c.75T>C (p.Pro25=)]
NM_000551.4(VHL):c.75T>C (p.Pro25=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024