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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
PubMed
Summary
This summary is machine-generated.

Interpreting genetic variants in cancer is challenging. DyVarMap, a new framework, uses structural dynamics to predict variant effects, offering mechanistic insights for precision oncology.

Keywords:
AlphaFold2FGFR2conformational dynamicsmachine learningmissense variantprecision oncologyreceptor tyrosine kinasevariant effect prediction

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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.