NM_173477.5(USH1G):c.1200C>T (p.His400=) AND not provided
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 18, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001497836.7
Allele description [Variation Report for NM_173477.5(USH1G):c.1200C>T (p.His400=)]
NM_173477.5(USH1G):c.1200C>T (p.His400=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024