c.460+16G>T
SpliceS3Likely benignCytoplasmic · predictedS3 — Cryptic donor activation predicted (SpliceAI ΔS 0.21)
Interactive 3D Structure
AlphaFold wild-type wolframin · the variant site near residue 154 (N-terminal cytoplasmic (intrinsically disordered)) is highlighted.
Variant Assessment
Therapeutic Implication · S3
Clinical Evidence
Not observed in ~730k individuals — consistent with a rare allele (ACMG PM2_supporting).
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Full Variant Card
c.460+16G_T — WFS1 Molecular Atlas Card
Variant type: Splice site Boundary: donor (5' splice site) · intronic offset +16 Nearest protein position: ~154 (N-terminal cytoplasmic (intrinsically disordered))
Schema category: S3 — Cryptic donor activation predicted (SpliceAI ΔS 0.21)
SpliceAI's strongest signal is a NEW cryptic donor site (ΔS 0.21, ~-6 nt from the variant; acceptor-gain 0.00, acceptor-loss 0.00, donor-gain 0.21, donor-loss 0.00). Cryptic activation produces a non-canonical junction whose reading-frame impact depends on the exact cryptic position — typically a partial exon gain/loss. Outcome is context-dependent; wet-lab RNA validation required. Flagged S3.
Splice prediction
- Affected site: donor (5' splice site), extended splice region
- SpliceAI delta scores (GRCh38 chr4:6289147 G>T):
- acceptor gain 0.00 · acceptor loss 0.00
- donor gain 0.21 · donor loss 0.00
- Predicted outcome: Cryptic donor activation predicted (SpliceAI ΔS 0.21)
Clinical evidence
- Classification: Likely benign
- Review status: criteria provided, single submitter
- cDNA change: c.460+16G>T
- ClinVar accession: VCV003607857
- Last evaluated: 2025/02/03 00:00
- Submissions: 1
Card generated by wolfram-atlas-batch (splice pipeline) on 2026-06-08T07:50:31.536741Z.
Schema: reference/card_schema_extension.md (S1–S3). WFS1: UniProt O76024, AlphaFold v6.