NM_000260.4(MYO7A):c.2366T>C (p.Leu789Pro) AND Usher syndrome type 1B
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 16, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001279400.1
Allele description [Variation Report for NM_000260.4(MYO7A):c.2366T>C (p.Leu789Pro)]
NM_000260.4(MYO7A):c.2366T>C (p.Leu789Pro)
Condition(s)
- Name:
- Usher syndrome type 1B (USH1B)
- Synonyms:
- Usher syndrome type IB
- Identifiers:
- MONDO: MONDO:0700087; MedGen: C2931206
Assertion and evidence details
Last Updated: Aug 13, 2023