NM_021625.5(TRPV4):c.1378C>T (p.Arg460Trp) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Nov 19, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002379021.2
Allele description [Variation Report for NM_021625.5(TRPV4):c.1378C>T (p.Arg460Trp)]
NM_021625.5(TRPV4):c.1378C>T (p.Arg460Trp)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Jun 17, 2024