A curated census of pathogenic and likely pathogenic UTR variants and evaluation of deep learning models for variant effect prediction

Emma Bohn; Tammy T Y Lau; Omar Wagih; Tehmina Masud; Daniele Merico

doi:10.3389/fmolb.2023.1257550

A curated census of pathogenic and likely pathogenic UTR variants and evaluation of deep learning models for variant effect prediction

Front Mol Biosci. 2023 Sep 8:10:1257550. doi: 10.3389/fmolb.2023.1257550. eCollection 2023.

Authors

Emma Bohn^#¹, Tammy T Y Lau^#¹, Omar Wagih¹, Tehmina Masud¹, Daniele Merico^{1

2}

Affiliations

¹ Deep Genomics Inc., Toronto, ON, Canada.
² The Centre for Applied Genomics, Hospital for Sick Children, Toronto, ON, Canada.

^# Contributed equally.

Abstract

Introduction: Variants in 5' and 3' untranslated regions (UTR) contribute to rare disease. While predictive algorithms to assist in classifying pathogenicity can potentially be highly valuable, the utility of these tools is often unclear, as it depends on carefully selected training and validation conditions. To address this, we developed a high confidence set of pathogenic (P) and likely pathogenic (LP) variants and assessed deep learning (DL) models for predicting their molecular effects. Methods: 3' and 5' UTR variants documented as P or LP (P/LP) were obtained from ClinVar and refined by reviewing the annotated variant effect and reassessing evidence of pathogenicity following published guidelines. Prediction scores from sequence-based DL models were compared between three groups: P/LP variants acting though the mechanism for which the model was designed (model-matched), those operating through other mechanisms (model-mismatched), and putative benign variants. PhyloP was used to compare conservation scores between P/LP and putative benign variants. Results: 295 3' and 188 5' UTR variants were obtained from ClinVar, of which 26 3' and 68 5' UTR variants were classified as P/LP. Predictions by DL models achieved statistically significant differences when comparing modelmatched P/LP variants to both putative benign variants and modelmismatched P/LP variants, as well as when comparing all P/LP variants to putative benign variants. PhyloP conservation scores were significantly higher among P/LP compared to putative benign variants for both the 3' and 5' UTR. Discussion: In conclusion, we present a high-confidence set of P/LP 3' and 5' UTR variants spanning a range of mechanisms and supported by detailed pathogenicity and molecular mechanism evidence curation. Predictions from DL models further substantiate these classifications. These datasets will support further development and validation of DL algorithms designed to predict the functional impact of variants that may be implicated in rare disease.

Keywords: deep learning; non-coding variation; rare disease; untranslated region (UTR); variant classification.

Grants and funding

The authors declare financial support was received for the research, authorship, and/or publication of this article. This study was funded by Deep Genomics Inc.