TSNAX-DT

Chr 1

TSNAX divergent transcript

I cannot provide a clinical summary for TSNAX-DT as no functional or phenotypic information has been provided in the data. TSNAX-DT appears to be a transcript designation, but without details about protein function, associated diseases, or inheritance patterns, a clinically meaningful summary cannot be written according to the specified guidelines.

Clinical SummaryTSNAX-DT
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ClinVar Variants
16 unique Pathogenic / Likely Pathogenic of 16 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

16 submitted variants in ClinVar

Classification Summary

Pathogenic15
Likely Pathogenic1
15
Pathogenic
1
Likely Pathogenic

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
15
Likely Pathogenic
1
VUS
0
Likely Benign
0
Benign
0
Total16

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

TSNAX-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.

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

No open access results found