Method | Authors' Recommended Pathogenicity threshold | Misclassified known pathogenic variants |
---|---|---|
SIFT | < 0.05 | 38% |
> 0.8 | 31% | |
CADD | > 20 | 26% |
MetaLR | > 0.5 | 27% |
> 0.025 | 5% |
Enter the GRCh37/hg19 coordinate for a missense variant to retrieve its
{{allele.alt}} | {{allele.mcap | number:3}} | Likely Benign Possibly Pathogenic |
Jagadeesh, K., Wenger, A., Berger, M., Guturu, H., Stenson, P., Cooper, D., Bernstein, J., and Bejerano, G. (2016). M-CAP eliminates a majority of variants with uncertain significance in clinical exomes at high sensitivity. Nature Genetics, 2016. 48 (12) 1581 DOI: 10.1038/ng.3703
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