NM_001113378.2(FANCI):c.1797T>C (p.Ala599=) AND Fanconi anemia complementation group I
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 21, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002506855.1
Allele description [Variation Report for NM_001113378.2(FANCI):c.1797T>C (p.Ala599=)]
NM_001113378.2(FANCI):c.1797T>C (p.Ala599=)
Condition(s)
Assertion and evidence details
Last Updated: Feb 20, 2024