NM_000551.4(VHL):c.598C>T (p.Arg200Trp) AND not specified
- Germline classification:
- Uncertain significance (2 submissions)
- Last evaluated:
- Jul 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000122262.15
Allele description [Variation Report for NM_000551.4(VHL):c.598C>T (p.Arg200Trp)]
NM_000551.4(VHL):c.598C>T (p.Arg200Trp)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024