NM_153676.4(USH1C):c.1859G>T (p.Arg620Leu) AND not specified
- Germline classification:
- Benign (3 submissions)
- Last evaluated:
- Mar 27, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000152545.9
Allele description [Variation Report for NM_153676.4(USH1C):c.1859G>T (p.Arg620Leu)]
NM_153676.4(USH1C):c.1859G>T (p.Arg620Leu)
Condition(s)
- Synonyms:
- AllHighlyPenetrant
- Identifiers:
- MedGen: CN169374
Assertion and evidence details
Last Updated: Sep 29, 2024