CNNM3-DT

Chr 2

CNNM3 divergent transcript

I cannot provide a clinical summary for CNNM3-DT as no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data below the prompt. Without this essential clinical information, I cannot write an accurate summary following the specified guidelines.

Clinical SummaryCNNM3-DT
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ClinVar Variants
11 unique Pathogenic / Likely Pathogenic· 11 VUS of 23 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

23 submitted variants in ClinVar

Classification Summary

Pathogenic10
Likely Pathogenic1
VUS11
Likely Benign1
10
Pathogenic
1
Likely Pathogenic
11
VUS
1
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
10
Likely Pathogenic
1
VUS
11
Likely Benign
1
Benign
0
Total23

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

CNNM3-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