NM_001371596.2(MFSD8):c.235G>T (p.Val79Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 11, 2016
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002318662.9
Allele description [Variation Report for NM_001371596.2(MFSD8):c.235G>T (p.Val79Phe)]
NM_001371596.2(MFSD8):c.235G>T (p.Val79Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
Assertion and evidence details
Last Updated: Nov 10, 2024