APC

Tumor-predisposition control/caution

MANE transcriptENST00000257430.9
ClinVar P/LP records2556
Low-record-burden flagno
Unit rows85

Unit-level record coverage

Unit typeBest record coverageEstimated payload
Single exon63.8%8,687 bp
Adjacent exon block75.5%9,237 bp
Downstream-CDS99.6%8,529 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
Familial adenomatous polyposis 12,057Tumor-predisposition control context0.7472050.991736
Hereditary cancer-predisposing syndrome1,035Tumor-predisposition control context0.7371980.991304
Familial multiple polyposis syndrome150Tumor-predisposition control context0.6666670.986667
Carcinoma of colon97Tumor-predisposition control context0.6185570.938144
Classic or attenuated familial adenomatous polyposis66Tumor-predisposition control context0.7272730.939394
Desmoid disease, hereditary43Tumor-predisposition control context0.4883720.953488
Gastric cancer40Tumor-predisposition control context0.6000001.000000
Colorectal cancer40Tumor-predisposition control context0.5500001.000000

View condition-facet overview and downloads