NM_001710.6(CFB):c.1398C>T (p.Tyr466=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- May 6, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002948539.2
Allele description [Variation Report for NM_001710.6(CFB):c.1398C>T (p.Tyr466=)]
NM_001710.6(CFB):c.1398C>T (p.Tyr466=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Feb 14, 2024