NM_001386140.1(MTTP):c.2657C>T (p.Pro886Leu) AND Abetalipoproteinaemia
- Germline classification:
- Conflicting interpretations of pathogenicity (7 submissions)
- Last evaluated:
- Feb 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000601949.15
Allele description [Variation Report for NM_001386140.1(MTTP):c.2657C>T (p.Pro886Leu)]
NM_001386140.1(MTTP):c.2657C>T (p.Pro886Leu)
Condition(s)
- Name:
- Abetalipoproteinaemia (ABL)
- Synonyms:
- MTP DEFICIENCY; Abetalipoproteinemia; Bassen Kornzweig syndrome; See all synonyms [MedGen]
- Identifiers:
- MONDO: MONDO:0008692; MedGen: C0000744; Orphanet: 14; OMIM: 200100; Human Phenotype Ontology: HP:0008181
Assertion and evidence details
Last Updated: Oct 13, 2024