DyVarMap: Integrating Conformational Dynamics and Interpretable Machine Learning for Cancer-Associated Missense
Yiyang Lian1, Amarda Shehu1,2
1School of Systems Biology, George Mason University, Manassas, VA 20110, USA.
Bioengineering (Basel, Switzerland)
|January 28, 2026
Summary
Interpreting genetic variants in cancer is challenging. DyVarMap, a new framework, uses structural dynamics to predict variant effects, offering mechanistic insights for precision oncology.
Area of Science:
- Computational biology
- Structural bioinformatics
- Precision oncology
Background:
- Interpreting missense variants in cancer genes is difficult, with many classified as variants of uncertain significance (VUS).
- Receptor tyrosine kinases like FGFR2 have functions dependent on conformational dynamics, complicating variant analysis.
- Existing sequence-based predictors often lack mechanistic explanations for variant effects.
Purpose of the Study:
- To develop DyVarMap, an interpretable structural-learning framework for predicting the pathogenicity of cancer-associated gene variants.
- To integrate conformational dynamics into variant effect prediction for improved accuracy and mechanistic understanding.
- To provide testable hypotheses for experimental validation in precision oncology.
Main Methods:
- DyVarMap integrates AlphaFold2-based ensemble generation with physics-driven refinement and manifold learning.
- A supervised classification model uses five biophysically motivated geometric features.
- SHAP analysis provides mechanistic attributions for variant pathogenicity predictions.
Main Results:
- DyVarMap successfully classified pathogenicity for FGFR2 variants, generating diverse conformational ensembles and identifying metastable states.
- External validation on ten kinase-domain variants achieved an AUROC of 0.77 with superior calibration compared to PolyPhen-2 and AlphaMissense.
- Feature importance analysis highlighted K659-E565 salt-bridge distance and DFG motif dihedral angles as key predictors, linking predictions to known activation mechanisms.
Conclusions:
- DyVarMap effectively bridges the gap between static structure prediction and dynamics-aware functional assessment.
- The framework provides structurally coherent mechanistic explanations for variant effects, aiding in precision oncology.
- Incorporating conformational dynamics into variant effect prediction offers significant value for clinical applications and experimental validation.
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