NM_001278716.2(FBXL4):c.422A>G (p.His141Arg) AND Inborn genetic diseases
- Germline classification:
- Uncertain significance (1 submission)
- Last evaluated:
- May 11, 2022
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV002894289.2
Allele description [Variation Report for NM_001278716.2(FBXL4):c.422A>G (p.His141Arg)]
NM_001278716.2(FBXL4):c.422A>G (p.His141Arg)
Condition(s)
- Name:
- Inborn genetic diseases
- Identifiers:
- MeSH: D030342; MedGen: C0950123
-
Rattus norvegicus insulin induced gene 1, mRNA (cDNA clone MGC:93442 IMAGE:71252...
Rattus norvegicus insulin induced gene 1, mRNA (cDNA clone MGC:93442 IMAGE:7125208), complete cdsgi|50925490|gb|BC078827.1|Nucleotide
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See more...Assertion and evidence details
Last Updated: Sep 29, 2024