NM_001277062.2(MFF):c.205T>G (p.Ser69Ala) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jun 23, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003348711.2
Allele description [Variation Report for NM_001277062.2(MFF):c.205T>G (p.Ser69Ala)]
NM_001277062.2(MFF):c.205T>G (p.Ser69Ala)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
BID BH3 interacting domain death agonist [Homo sapiens]
BID BH3 interacting domain death agonist [Homo sapiens]Gene ID:637Gene
-
Gene Links for GEO Profiles (Select 110701276) (1)
Gene
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Last Updated: May 1, 2024