NM_003718.5(CDK13):c.2084T>C (p.Ile695Thr) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Aug 8, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002928058.2
Allele description [Variation Report for NM_003718.5(CDK13):c.2084T>C (p.Ile695Thr)]
NM_003718.5(CDK13):c.2084T>C (p.Ile695Thr)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Sep 29, 2024