FKRP
Compact downstream-CDS record-coverage hypothesis
| MANE transcript | ENST00000318584.10 |
|---|---|
| ClinVar P/LP records | 224 |
| Low-record-burden flag | no |
| Unit rows | 13 |
Unit-level record coverage
| Unit type | Best record coverage | Estimated payload |
|---|---|---|
| Single exon | 99.6% | 3,164 bp |
| Adjacent exon block | 99.6% | 3,315 bp |
| Downstream-CDS | 100.0% | 1,485 bp |
Why this classification?
- Downstream-CDS record coverage is 100.0% with an estimated payload of 1,485 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 |
|---|---|---|---|---|
| Walker-Warburg congenital muscular dystrophy | 145 | Local compact architecture | 0.993103 | 0.993103 |
| Autosomal recessive limb-girdle muscular dystrophy type 2I | 97 | Local compact architecture | 1.000000 | 1.000000 |
| Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A5 | 85 | Local compact architecture | 1.000000 | 1.000000 |
| Muscular dystrophy-dystroglycanopathy type B5 | 36 | Local compact architecture | 1.000000 | 1.000000 |
| Cardiovascular phenotype | 23 | Local compact architecture | 1.000000 | 1.000000 |