SLC26A4

Compact downstream-CDS record-coverage hypothesis

MANE transcriptENST00000644269.2
ClinVar P/LP records631
Low-record-burden flagno
Unit rows115

Unit-level record coverage

Unit typeBest record coverageEstimated payload
Single exon8.9%114 bp
Adjacent exon block33.6%768 bp
Downstream-CDS100.0%2,340 bp

Why this classification?

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 labelP/LP recordsCondition architectureLocal coverageBoundary-CDS coverage
Autosomal recessive nonsyndromic hearing loss 4389Boundary-CDS payload architecture0.3213371.000000
Pendred syndrome318Boundary-CDS payload architecture0.3301891.000000
Rare genetic deafness62Boundary-CDS payload architecture0.3870971.000000
SLC26A4-related disorder25Boundary-CDS payload architecture0.4000001.000000

View condition-facet overview and downloads