NM_007217.4(PDCD10):c.630T>C (p.Thr210=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 1, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002353973.2
Allele description [Variation Report for NM_007217.4(PDCD10):c.630T>C (p.Thr210=)]
NM_007217.4(PDCD10):c.630T>C (p.Thr210=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: May 1, 2024