c.232+15T>A
SpliceS3Likely benignCytoplasmic · predictedS3 — Minimal predicted splicing impact (SpliceAI ΔS 0.01)
Interactive 3D Structure
AlphaFold wild-type wolframin · the variant site near residue 78 (N-terminal cytoplasmic (intrinsically disordered)) is highlighted.
Variant Assessment
Therapeutic Implication · S3
Clinical Evidence
Observed at very low frequency in gnomAD.
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Download the c.232+15T>A card below and upload it to Wolfram Intelligence to generate therapeutic-strategy proposals matched to this S3 splice variant and its domain context.
Full Variant Card
c.232+15T_A — WFS1 Molecular Atlas Card
Variant type: Splice site Boundary: donor (5' splice site) · intronic offset +15 Nearest protein position: ~78 (N-terminal cytoplasmic (intrinsically disordered))
Schema category: S3 — Minimal predicted splicing impact (SpliceAI ΔS 0.01)
SpliceAI predicts little splicing disruption at this donor (5') site (max ΔS 0.01 < 0.2; acceptor-gain 0.00, acceptor-loss 0.00, donor-gain 0.00, donor-loss 0.01). The variant may be tolerated or act through a weak/again-tissue-specific mechanism; wet-lab RNA validation is the arbiter before any therapeutic call.
Splice prediction
- Affected site: donor (5' splice site), extended splice region
- SpliceAI delta scores (GRCh38 chr4:6277702 T>A):
- acceptor gain 0.00 · acceptor loss 0.00
- donor gain 0.00 · donor loss 0.01
- Predicted outcome: Minimal predicted splicing impact (SpliceAI ΔS 0.01)
Clinical evidence
- Classification: Likely benign
- Review status: criteria provided, single submitter
- cDNA change: c.232+15T>A
- ClinVar accession: VCV002834692
- Last evaluated: 2023/07/08 00:00
- Submissions: 1
Card generated by wolfram-atlas-batch (splice pipeline) on 2026-06-08T07:49:37.239732Z.
Schema: reference/card_schema_extension.md (S1–S3). WFS1: UniProt O76024, AlphaFold v6.