NM_014874.4(MFN2):c.2179C>T (p.Leu727Phe) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 12, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV004417037.1
Allele description [Variation Report for NM_014874.4(MFN2):c.2179C>T (p.Leu727Phe)]
NM_014874.4(MFN2):c.2179C>T (p.Leu727Phe)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
FAS-associated death domain protein-like [Salmo trutta]
FAS-associated death domain protein-like [Salmo trutta]gi|1696175588|ref|XP_029622911.1|Protein
-
ABC transporter ATP-binding protein [Sneathiella marina]
ABC transporter ATP-binding protein [Sneathiella marina]gi|2254874830|gnl|PRJNA844166|NBZ79 5|gb|USG61056.1|Protein
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Last Updated: May 7, 2024