NM_004628.5(XPC):c.1734C>A (p.Val578=) AND not provided
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 30, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000894251.9
Allele description [Variation Report for NM_004628.5(XPC):c.1734C>A (p.Val578=)]
NM_004628.5(XPC):c.1734C>A (p.Val578=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024