NM_000136.3(FANCC):c.1485G>A (p.Leu495=) AND Fanconi anemia complementation group C
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Jul 7, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001167959.14
Allele description [Variation Report for NM_000136.3(FANCC):c.1485G>A (p.Leu495=)]
NM_000136.3(FANCC):c.1485G>A (p.Leu495=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 23, 2024