ARHGAP11B-DT

Chr 15

ARHGAP11B divergent transcript

NCBI Gene: 102725021ENSG00000247728
66
ClinVar variants
46
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— ARHGAP11B-DT
📋
ClinVar Variants
46 Pathogenic / Likely Pathogenic· 13 VUS of 66 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

66 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic44
Likely Pathogenic2
VUS13
Likely Benign2
Conflicting5
44
Pathogenic
2
Likely Pathogenic
13
VUS
2
Likely Benign
5
Conflicting

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————44
Likely Pathogenic
————2
VUS
————13
Likely Benign
————2
Benign
————0
Conflicting
—5
Total—66

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

ARHGAP11B-DT · protein map & ClinVar variants

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

OMIM — Genotype-Phenotype

OMIM

No OMIM entries found.

Clinical Literature
Landmark / reviewRecent case evidence

No publications found for ARHGAP11B-DT

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