NM_001018113.3(FANCB):c.2477C>T (p.Thr826Met) AND Fanconi anemia complementation group B
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001167168.4
Allele description [Variation Report for NM_001018113.3(FANCB):c.2477C>T (p.Thr826Met)]
NM_001018113.3(FANCB):c.2477C>T (p.Thr826Met)
Condition(s)
Assertion and evidence details
Last Updated: Apr 15, 2024