NM_004629.2(FANCG):c.1718G>T (p.Arg573Met) AND Fanconi anemia
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Aug 20, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001300972.2
Allele description [Variation Report for NM_004629.2(FANCG):c.1718G>T (p.Arg573Met)]
NM_004629.2(FANCG):c.1718G>T (p.Arg573Met)
Condition(s)
Assertion and evidence details
Last Updated: Nov 25, 2023