NM_032119.4(ADGRV1):c.11390C>T (p.Thr3797Ile) AND Usher syndrome type 2C
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 13, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001157315.4
Allele description [Variation Report for NM_032119.4(ADGRV1):c.11390C>T (p.Thr3797Ile)]
NM_032119.4(ADGRV1):c.11390C>T (p.Thr3797Ile)
Condition(s)
Assertion and evidence details
Last Updated: Feb 28, 2024