NM_001710.6(CFB):c.405C>T (p.Tyr135=) AND Atypical hemolytic-uremic syndrome with B factor anomaly
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000301807.5
Allele description [Variation Report for NM_001710.6(CFB):c.405C>T (p.Tyr135=)]
NM_001710.6(CFB):c.405C>T (p.Tyr135=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024