NM_000380.4(XPA):c.696C>T (p.Ser232=) AND not provided
- Germline classification:
- Likely benign (2 submissions)
- Last evaluated:
- Feb 1, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000977628.13
Allele description
NM_000380.4(XPA):c.696C>T (p.Ser232=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jul 15, 2024