NM_016356.5(DCDC2):c.543C>T (p.Ser181=) AND multiple conditions
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 29, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001088737.6
Allele description [Variation Report for NM_016356.5(DCDC2):c.543C>T (p.Ser181=)]
NM_016356.5(DCDC2):c.543C>T (p.Ser181=)
Condition(s)
Assertion and evidence details
Last Updated: Mar 16, 2024