NM_033380.3(COL4A5):c.4223C>G (p.Thr1408Ser) AND X-linked Alport syndrome
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Nov 11, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001832185.1
Allele description [Variation Report for NM_033380.3(COL4A5):c.4223C>G (p.Thr1408Ser)]
NM_033380.3(COL4A5):c.4223C>G (p.Thr1408Ser)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024