NM_000391.4(TPP1):c.465T>C (p.His155=) AND Inborn genetic diseases
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Apr 6, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002315415.9
Allele description [Variation Report for NM_000391.4(TPP1):c.465T>C (p.His155=)]
NM_000391.4(TPP1):c.465T>C (p.His155=)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Aug 18, 2024