Variants
Sign InSign Up

rs1057521176

  • Likely pathogenic

Your Genotype

Sign In

Description

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

© 2024 Biocodify. All rights reserved.

TwitterTwitter

Product

HomePricingDashboard

Stay up to date

The latest news and updates from Biocodify, sent to your inbox.