NM_000136.3(FANCC):c.407A>C (p.Gln136Pro) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Nov 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001593904.5
Allele description [Variation Report for NM_000136.3(FANCC):c.407A>C (p.Gln136Pro)]
NM_000136.3(FANCC):c.407A>C (p.Gln136Pro)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: May 1, 2024