NM_001018115.3(FANCD2):c.2148C>G (p.Thr716=) AND Fanconi anemia
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 31, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000230340.15
Allele description [Variation Report for NM_001018115.3(FANCD2):c.2148C>G (p.Thr716=)]
NM_001018115.3(FANCD2):c.2148C>G (p.Thr716=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 20, 2024