NM_000136.3(FANCC):c.*213T>G AND Fanconi anemia complementation group C
- Germline classification:
- Likely 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:
- RCV001167355.4
Allele description [Variation Report for NM_000136.3(FANCC):c.*213T>G]
NM_000136.3(FANCC):c.*213T>G
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023