NM_004629.2(FANCG):c.1794C>G (p.Ser598Arg) AND Fanconi anemia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 17, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002890870.2
Allele description [Variation Report for NM_004629.2(FANCG):c.1794C>G (p.Ser598Arg)]
NM_004629.2(FANCG):c.1794C>G (p.Ser598Arg)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024