NM_000278.5(PAX2):c.886G>A (p.Val296Met) AND PAX2-related disorder
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004536551.1
Allele description [Variation Report for NM_000278.5(PAX2):c.886G>A (p.Val296Met)]
NM_000278.5(PAX2):c.886G>A (p.Val296Met)
Condition(s)
- Name:
- PAX2-related disorder
- Identifiers:
Assertion and evidence details
Last Updated: Aug 11, 2024