@genebe/pangolin
Latest release Active PublicPangolin masked splice gain/loss scores
About pangolin
Pangolin masked splice gain/loss scores
This annotation contains compact Pangolin scores for all precomputed GRCh38 SNVs in protein-coding genes. Pangolin predicts changes in splice-site usage; the source scores were calculated with the default 50-nucleotide window and masked using GENCODE splice-site annotations.
For each genomic SNV, the builder selects the source record with the largest raw max_score = max(gain_score, loss_score). Scores smaller than 0.1 are omitted with their corresponding relative position to reduce storage: gain_score and gain_pos are both NULL below the gain threshold, and the same rule applies to loss. max_score is always retained and is calculated before this thresholding.
Source and citation
Wagner N, Neverov A. Pangolin precomputed scores. Zenodo, version 1 (2025). https://doi.org/10.5281/zenodo.15649338
Zeng T, Li YI. Predicting RNA splicing from DNA sequence using Pangolin. Genome Biology. 2022;23:103. https://doi.org/10.1186/s13059-022-02664-4
Genome Reference & Assembly
This database is compiled for homo_sapiens using reference assembly GRCh38.
License Acceptance Required
Using or annotating with this database requires explicitly accepting the Not Specified terms in your Genebe client pipeline or API queries.
Metadata & Attributes
- Maintainer / Owner @genebe
- Database Type Variant Annotation
- Genome Assembly homo_sapiens (GRCh38)
- License Not Specified
- Created Date 12 Sept 2026, 10:49:34 UTC