SEPTIN7-DT

Chr 7

SEPTIN7 divergent transcript

Also known as: SEPT7-AS1, SEPTIN7-AS1

NCBI Gene: 101928545ENSG00000228878
6
ClinVar variants
6
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— SEPTIN7-DT
📋
ClinVar Variants
6 Pathogenic / Likely Pathogenic of 6 total submissions
Some data sources returned errors (1)

omim: Error: OMIM fetch failed: 429

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

6 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic6
6
Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————6
Likely Pathogenic
————0
VUS
————0
Likely Benign
————0
Benign
————0
Total—6

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

SEPTIN7-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 SEPTIN7-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