NM_000384.3(APOB):c.6261C>A (p.Thr2087=) AND not provided
- Germline classification:
- Benign/Likely benign (3 submissions)
- Last evaluated:
- Apr 1, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000759462.19
Allele description [Variation Report for NM_000384.3(APOB):c.6261C>A (p.Thr2087=)]
NM_000384.3(APOB):c.6261C>A (p.Thr2087=)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Apr 20, 2024