NM_000092.5(COL4A4):c.507G>C (p.Lys169Asn) AND Alport syndrome
- Germline classification:
- Uncertain significance (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:
- RCV001142916.5
Allele description [Variation Report for NM_000092.5(COL4A4):c.507G>C (p.Lys169Asn)]
NM_000092.5(COL4A4):c.507G>C (p.Lys169Asn)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024