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Pangolin masked splice gain/loss scores

Labels: splicing variant-effect pangolin masked
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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
For research and educational, non-commercial use only. Not for clinical or diagnostic use. GeneBe does not provide medical advice. Data use for AI modeling is prohibited: if used, the cost is $0.001 per byte of downloaded uncompressed data.