rs2061304701
- Uncertain significance
Your Genotype
Sign InDescription
This sequence change results in a premature translational stop signal in the BRIP1 gene (p.Cys1164*). While this is not anticipated to result in nonsense mediated decay, it is expected to disrupt the last 86 amino acids of the BRIP1 protein. This variant is not present in population databases (ExAC no frequency). This variant has not been reported in the literature in individuals with BRIP1-related conditions. Experimental studies and prediction algorithms are not available or were not evaluated, and the functional significance of this variant is currently unknown. In summary, the available evidence is currently insufficient to determine the role of this variant in disease. Therefore, it has been classified as a Variant of Uncertain Significance.
Reference Allele
G
Alternative Allele
T
Chromosome
17
Location
61683554
Variant Type
SNP
Genes
ClinVar
Name
NM_032043.3(BRIP1):c.3492C>A (p.Cys1164Ter)
Allele
T
Clinical Significance
Uncertain significance