NM_000098.3(CPT2):c.1851T>C (p.His617=) AND Encephalopathy, acute, infection-induced, susceptibility to, 4
- Germline classification:
- Benign (1 submission)
- Last evaluated:
- Apr 11, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003451515.1
Allele description [Variation Report for NM_000098.3(CPT2):c.1851T>C (p.His617=)]
NM_000098.3(CPT2):c.1851T>C (p.His617=)
Condition(s)
Assertion and evidence details
Last Updated: Oct 8, 2024