ACAD9-DT

Chr 3

ACAD9 divergent transcript

NCBI Gene: 123706524ENSG00000287110

ResearchGenerating clinical summary…
Clinical Summary— ACAD9-DT
📋
ClinVar Variants
3 total variants — no pathogenic classifications of 3 total submissions
Explore recent and relevant literature in Research Assistant →
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

3 submitted variants in ClinVar

ClinVar

Classification Summary

Likely Benign2
Benign1
2
Likely Benign
1
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories· variant type breakdown unavailable

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————0
Likely Pathogenic
————0
VUS
————0
Likely Benign
————2
Benign
————1
Total—3

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

4 pathogenic / likely-pathogenic (of 8) ClinVar copy-number / structural variants overlap ACAD9-DT — these span large chromosomal regions, not the gene specifically, and are excluded from the counts above. Explore in CNV tools →

Protein Context — Lollipop Plot

ACAD9-DT · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →

External Resources

Links to major genomics databases and tools

Franklin by Genoox
AI-powered variant curation and clinical analysis
DECIPHER
Genomic variants and phenotypes in rare disease patients