NM_032444.4(SLX4):c.2289T>C (p.Pro763=) AND Fanconi anemia complementation group P
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 22, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002498195.1
Allele description [Variation Report for NM_032444.4(SLX4):c.2289T>C (p.Pro763=)]
NM_032444.4(SLX4):c.2289T>C (p.Pro763=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 14, 2024