NM_153033.5(KCTD7):c.439C>T (p.Leu147=) AND Progressive myoclonic epilepsy type 3
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Oct 13, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001422339.4
Allele description [Variation Report for NM_153033.5(KCTD7):c.439C>T (p.Leu147=)]
NM_153033.5(KCTD7):c.439C>T (p.Leu147=)
Condition(s)
- Name:
- Progressive myoclonic epilepsy type 3
- Synonyms:
- EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITH OR WITHOUT INTRACELLULAR INCLUSIONS; CEROID LIPOFUSCINOSIS, NEURONAL, 14; EPILEPSY, PROGRESSIVE MYOCLONIC, 3, WITHOUT INTRACELLULAR INCLUSIONS
- Identifiers:
- MONDO: MONDO:0012721; MedGen: C2673257; Orphanet: 263516; OMIM: 611726
Assertion and evidence details
Last Updated: May 1, 2024