NM_000035.4(ALDOB):c.223G>A (p.Gly75Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Dec 15, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002954646.2
Allele description [Variation Report for NM_000035.4(ALDOB):c.223G>A (p.Gly75Arg)]
NM_000035.4(ALDOB):c.223G>A (p.Gly75Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
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Homo sapiens cDNA clone IMAGE:3961342, containing frame-shift errors
Homo sapiens cDNA clone IMAGE:3961342, containing frame-shift errorsgi|17512555|gb|BC019226.1|Nucleotide
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Homo sapiens UBX domain protein 10, mRNA (cDNA clone MGC:51306 IMAGE:5295853), c...
Homo sapiens UBX domain protein 10, mRNA (cDNA clone MGC:51306 IMAGE:5295853), complete cdsgi|28703991|gb|BC047428.1|Nucleotide
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BY244994 RIKEN full-length enriched, visual cortex Mus musculus cDNA clone K2300...
BY244994 RIKEN full-length enriched, visual cortex Mus musculus cDNA clone K230054A13 5', mRNA sequencegi|26426506|gnl|dbEST|15902916|dbj| 994.1|Nucleotide
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P120 antigen [Homo sapiens]
P120 antigen [Homo sapiens]gi|287723|emb|CAA39119.1|Protein
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Last Updated: Oct 13, 2024