NM_002085.5(GPX4):c.535C>T (p.Arg179Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Apr 17, 2023
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV003270192.2
Allele description [Variation Report for NM_002085.5(GPX4):c.535C>T (p.Arg179Cys)]
NM_002085.5(GPX4):c.535C>T (p.Arg179Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Chain L, NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial
Chain L, NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrialgi|2463610966|pdb|7W0Y|LProtein
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Last Updated: May 1, 2024