NM_001384140.1(PCDH15):c.1900G>A (p.Val634Ile) AND Usher syndrome type 1F
- Germline classification:
- Uncertain significance (3 submissions)
- 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:
- RCV001275398.4
Allele description [Variation Report for NM_001384140.1(PCDH15):c.1900G>A (p.Val634Ile)]
NM_001384140.1(PCDH15):c.1900G>A (p.Val634Ile)
Condition(s)
Assertion and evidence details
Last Updated: Oct 13, 2024