NM_000136.3(FANCC):c.1170C>G (p.Pro390=) AND FANCC-related condition
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003982972.1
Allele description [Variation Report for NM_000136.3(FANCC):c.1170C>G (p.Pro390=)]
NM_000136.3(FANCC):c.1170C>G (p.Pro390=)
Condition(s)
- Name:
- FANCC-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Mar 16, 2024