NM_001278716.2(FBXL4):c.1740_1742del (p.Leu581del) AND Inborn genetic diseases
- Germline classification:
- Likely pathogenic (1 submission)
- Last evaluated:
- Jun 8, 2018
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001267293.2
Allele description [Variation Report for NM_001278716.2(FBXL4):c.1740_1742del (p.Leu581del)]
NM_001278716.2(FBXL4):c.1740_1742del (p.Leu581del)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Homo sapiens ubiquitin specific peptidase 6 (USP6), transcript variant 2, mRNA
Homo sapiens ubiquitin specific peptidase 6 (USP6), transcript variant 2, mRNAgi|747019228|ref|NM_004505.3|Nucleotide
-
Severe acute respiratory syndrome coronavirus 2 isolate SARS-CoV-2/human/USA/CA-...
Severe acute respiratory syndrome coronavirus 2 isolate SARS-CoV-2/human/USA/CA-CZB-59X002/2020, complete genomegi|1835438350|gb|MT394528.1|Nucleotide
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Last Updated: Jan 7, 2023