NM_000135.4(FANCA):c.2606A>C (p.Gln869Pro) AND See cases
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Aug 31, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002252053.3
Allele description [Variation Report for NM_000135.4(FANCA):c.2606A>C (p.Gln869Pro)]
NM_000135.4(FANCA):c.2606A>C (p.Gln869Pro)
Condition(s)
- Name:
- See cases [See the Variation display for details]
- Identifiers:
Assertion and evidence details
Last Updated: May 12, 2024