NM_001384140.1(PCDH15):c.902C>T (p.Thr301Met) AND Usher syndrome type 1F
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jul 14, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001578650.2
Allele description [Variation Report for NM_001384140.1(PCDH15):c.902C>T (p.Thr301Met)]
NM_001384140.1(PCDH15):c.902C>T (p.Thr301Met)
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023