NM_000091.5(COL4A3):c.1353C>T (p.His451=) AND Alport syndrome
- Germline classification:
- Likely 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:
- RCV001138810.6
Allele description [Variation Report for NM_000091.5(COL4A3):c.1353C>T (p.His451=)]
NM_000091.5(COL4A3):c.1353C>T (p.His451=)
Condition(s)
Assertion and evidence details
Last Updated: Sep 29, 2024