NM_030787.4(CFHR5):c.832G>A (p.Gly278Ser) AND not provided
- Germline classification:
- Benign (2 submissions)
- Last evaluated:
- Jan 22, 2024
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000438250.9
Allele description [Variation Report for NM_030787.4(CFHR5):c.832G>A (p.Gly278Ser)]
NM_030787.4(CFHR5):c.832G>A (p.Gly278Ser)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Jun 17, 2024