NM_015404.4(WHRN):c.2348T>C (p.Val783Ala) AND Usher syndrome type 2D
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000278001.5
Allele description [Variation Report for NM_015404.4(WHRN):c.2348T>C (p.Val783Ala)]
NM_015404.4(WHRN):c.2348T>C (p.Val783Ala)
Condition(s)
Assertion and evidence details
Last Updated: Mar 10, 2024