STXBP1
Compact downstream-CDS record-coverage hypothesis
| MANE transcript | ENST00000373299.5 |
|---|---|
| ClinVar P/LP records | 400 |
| Low-record-burden flag | no |
| Unit rows | 103 |
Unit-level record coverage
| Unit type | Best record coverage | Estimated payload |
|---|---|---|
| Single exon | 12.0% | 155 bp |
| Adjacent exon block | 32.0% | 592 bp |
| Downstream-CDS | 98.5% | 1,745 bp |
Why this classification?
- Downstream-CDS record coverage is 98.5% with an estimated payload of 1,745 bp (≤5 kb).
- This label is boundary-based: high coverage can occur when many coding records lie downstream of an early transcript boundary.
How to read this page
Record coverage summarizes ClinVar P/LP records mapped to this gene. It does not estimate patient coverage, editing efficiency, therapeutic efficacy, or safety.
Downstream-CDS values are transcript-boundary hypotheses. High downstream coverage can be boundary-driven and should be read with payload and context burden.
Condition-associated pathogenic-record groups
Record-level ClinVar condition facets. These are not patient cohorts, disease prevalence, or patient coverage.
| Condition label | P/LP records | Condition architecture | Local coverage | Boundary-CDS coverage |
|---|---|---|---|---|
| Developmental and epileptic encephalopathy, 4 | 165 | Boundary-CDS payload architecture | 0.333333 | 0.957576 |
| Early-infantile DEE | 134 | Boundary-CDS payload architecture | 0.335821 | 0.977612 |
| Infantile epilepsy syndrome | 40 | Boundary-CDS payload architecture | 0.375000 | 0.950000 |
| Inborn genetic diseases | 26 | Boundary-CDS payload architecture | 0.423077 | 1.000000 |