NM_032043.3(BRIP1):c.251T>A (p.Leu84Ter) AND multiple conditions
- Germline classification:
- Pathogenic (1 submission)
- Last evaluated:
- Mar 8, 2020
- Review status:
- Somatic classification
of clinical impact: - None
- Review status:
- Somatic classification
of oncogenicity: - None
- Review status:
- Record status:
- current
- Accession:
- RCV001381413.6
Allele description [Variation Report for NM_032043.3(BRIP1):c.251T>A (p.Leu84Ter)]
NM_032043.3(BRIP1):c.251T>A (p.Leu84Ter)
Condition(s)
-
Homo sapiens selenoprotein N (SELENON), transcript variant 2, mRNA
Homo sapiens selenoprotein N (SELENON), transcript variant 2, mRNAgi|1519315052|ref|NM_020451.3|Nucleotide
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Last Updated: Sep 29, 2024