NM_000029.4(AGT):c.*226T>C AND Renal tubular dysgenesis
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Jan 12, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001098249.5
Allele description [Variation Report for NM_000029.4(AGT):c.*226T>C]
NM_000029.4(AGT):c.*226T>C
Condition(s)
- Name:
- Renal tubular dysgenesis
- Synonyms:
- Primitive renal tubule syndrome; Renotubular dysgenesis
- Identifiers:
- MONDO: MONDO:0017609; MedGen: C0266313; Human Phenotype Ontology: HP:0008660
-
Mus musculus NOD-derived CD11c +ve dendritic cells cDNA, RIKEN full-length enric...
Mus musculus NOD-derived CD11c +ve dendritic cells cDNA, RIKEN full-length enriched library, clone:F630002O05 product:ADP-ribosylation factor-like protein 7 (ADP-ribosylation factor-like protein LAK) homolog [Homo sapiens], full insert sequencegi|74199503|dbj|AK169890.1|Nucleotide
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Last Updated: Sep 16, 2024