NM_000384.3(APOB):c.3471T>C (p.Tyr1157=) AND APOB-related disorder
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Mar 29, 2019
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004544624.1
Allele description [Variation Report for NM_000384.3(APOB):c.3471T>C (p.Tyr1157=)]
NM_000384.3(APOB):c.3471T>C (p.Tyr1157=)
Condition(s)
- Name:
- APOB-related disorder
- Synonyms:
- APOB-Related Disorders; APOB-related condition
- Identifiers:
Assertion and evidence details
Last Updated: Jul 7, 2024