rs1057521176
- Likely pathogenic
Your Genotype
Sign InDescription
The D57E variant in the POLR3A gene has not been reported previously as a pathogenic variant, nor as a benign variant, to our knowledge. This variant was not observed in approximately 6500 individuals of European and African American ancestry in the NHLBI Exome Sequencing Project, indicating it is not a common benign variant in these populations. The D57E variant is a conservative amino acid substitution, which is not likely to impact secondary protein structure as these residues share similar properties; however, this substitution occurs at a position that is conserved across species, and in silico analysis predicts this variant is probably damaging to the protein structure/function. The D57E variant is a strong candidate for a pathogenic variant.
Reference Allele
G
Alternative Allele
C
Chromosome
10
Location
78026103
Variant Type
SNP
Genes
Phenotypes
ClinVar
Name
NM_007055.4(POLR3A):c.171C>G (p.Asp57Glu)
Allele
C
Clinical Significance
Likely pathogenic