CFAP95-DT

Chr 9

CFAP95 divergent transcript

Also known as: C9orf135-AS1, C9orf135-DT

I cannot provide a clinical summary for CFAP95-DT as no functional or clinical information was provided in the data. This appears to be a non-coding RNA or regulatory element rather than a protein-coding gene, but without specific details about its function, associated diseases, or inheritance patterns, I cannot write an accurate clinical summary.

Clinical SummaryCFAP95-DT
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ClinVar Variants
20 unique Pathogenic / Likely Pathogenic of 20 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

20 submitted variants in ClinVar

Classification Summary

Pathogenic17
Likely Pathogenic3
17
Pathogenic
3
Likely Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
17
Likely Pathogenic
3
VUS
0
Likely Benign
0
Benign
0
Total20

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

CFAP95-DT · protein map & ClinVar variants

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

3D Protein StructureAlphaFold

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Open Research Assistant →
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found