NM_004082.5(DCTN1):c.2389T>C (p.Phe797Leu) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 25, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002459546.9
Allele description [Variation Report for NM_004082.5(DCTN1):c.2389T>C (p.Phe797Leu)]
NM_004082.5(DCTN1):c.2389T>C (p.Phe797Leu)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024