NM_182758.4(WDR72):c.983A>G (p.Tyr328Cys) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- Feb 3, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002817918.2
Allele description [Variation Report for NM_182758.4(WDR72):c.983A>G (p.Tyr328Cys)]
NM_182758.4(WDR72):c.983A>G (p.Tyr328Cys)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Exudative vitreoretinopathy 7
Exudative vitreoretinopathy 7MedGen
-
C4539767[conceptid] (1)
MedGen
-
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC105372200), transcript varian...
PREDICTED: Homo sapiens uncharacterized lncRNA (LOC105372200), transcript variant X2, ncRNAgi|2217318634|ref|XR_935635.4|Nucleotide
-
putative secreted hydrolase [Streptomyces scabiei 87.22]
putative secreted hydrolase [Streptomyces scabiei 87.22]gi|260652008|emb|CBG75140.1|Protein
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Last Updated: May 1, 2024