NM_000551.4(VHL):c.147C>A (p.Gly49=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Dec 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003805509.1
Allele description [Variation Report for NM_000551.4(VHL):c.147C>A (p.Gly49=)]
NM_000551.4(VHL):c.147C>A (p.Gly49=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 5, 2024