NM_001386140.1(MTTP):c.2661T>A (p.Asp887Glu) AND not provided
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Oct 11, 2021
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001947341.3
Allele description [Variation Report for NM_001386140.1(MTTP):c.2661T>A (p.Asp887Glu)]
NM_001386140.1(MTTP):c.2661T>A (p.Asp887Glu)
Condition(s)
- Synonyms:
- none provided
- Identifiers:
- MedGen: C3661900
Assertion and evidence details
Last Updated: Sep 29, 2024