NM_001371596.2(MFSD8):c.1041A>G (p.Val347_Trp348=) AND Seizure
- Germline classification:
- Likely benign (1 submission)
- Last evaluated:
- Feb 21, 2017
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV000718223.2
Allele description
NM_001371596.2(MFSD8):c.1041A>G (p.Val347_Trp348=)
Condition(s)
- Name:
- Seizure
- Synonyms:
- Seizures
- Identifiers:
- MedGen: C0036572; Human Phenotype Ontology: HP:0001250
Assertion and evidence details
Last Updated: Sep 17, 2022