Note: Scoring of VCF files with CADD v1.7 is still rather slow if many new variants need to be calculated from scratch (e.g., if many insertion/deletion or multinucleotide subsitutions are included). If possible use the pre-scored whole genome and pre-calculated indel files directly where possible. We are very sorry for the inconvenience.
Multi SNV lookup
This form allows you to quickly access the score (and annotation) of multiple single nucleotide variants (SNV). If you are investigating longer ranges of CADD SNV scores, you might be interested in our UCSC Genome Browser Tracks for hg19/GRCh37 and hg38/GRCh38. Please note that copying and downloading of the annotation tables is not working in Internet Explorer.
CADD scores are freely available for all non-commercial applications. If you are planning on using them in a commercial application, please contact us.