NM_001384140.1(PCDH15):c.92-52T>G AND Usher syndrome type 1F
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jul 1, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001533583.2
Allele description [Variation Report for NM_001384140.1(PCDH15):c.92-52T>G]
NM_001384140.1(PCDH15):c.92-52T>G
Condition(s)
Assertion and evidence details
Last Updated: Dec 24, 2023