NM_000136.3(FANCC):c.147T>C (p.Tyr49=) AND Fanconi anemia
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 6, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001434646.6
Allele description [Variation Report for NM_000136.3(FANCC):c.147T>C (p.Tyr49=)]
NM_000136.3(FANCC):c.147T>C (p.Tyr49=)
Condition(s)
Assertion and evidence details
Last Updated: May 1, 2024