From: MutPred Splice: machine learning-based prediction of exonic variants that disrupt splicing
Data set | Proportion of SAVs in data set (predicted SAVs/total variants) | |
---|---|---|
Tumor suppressor | Oncogenes | |
Inherited disease | 25.3% (1,130/4,463) | 10.9% (132/1,207) |
Cancer | 16.0% (1,612/10,082) | 10.9% (525/4,831) |
1000 Genomes | 7.4% (84/1,133) | 8.0% (49/612) |