NM_000091.5(COL4A3):c.485A>G (p.Glu162Gly) AND Alport syndrome
- Germline classification:
- Benign (2 submissions)
- 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:
- RCV000295878.7
Allele description [Variation Report for NM_000091.5(COL4A3):c.485A>G (p.Glu162Gly)]
NM_000091.5(COL4A3):c.485A>G (p.Glu162Gly)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024