Input Data
Format: RefCodon AltCodon [Gene] [Description]
Results
Enter variant data and click "Analyze Batch" to see results.
Analyze genetic variants using RNAcube coordinates. Convert complex assessments to simple integer arithmetic.
Pathogenicity prediction becomes elementary arithmetic: |47 - 23| = 24, and 24 ≥ 16 = HIGH RISK. No protein structure needed.
Experimental thresholds based on RNAcube constraint analysis. Severity classifications may require validation with larger clinical datasets.
Enter variant data and click "Analyze Batch" to see results.