NM_000551.4(VHL):c.22T>G (p.Trp8Gly) AND not specified
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 27, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003230725.1
Allele description [Variation Report for NM_000551.4(VHL):c.22T>G (p.Trp8Gly)]
NM_000551.4(VHL):c.22T>G (p.Trp8Gly)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024