LCIIAR

Chr 15

lung cancer immune cell infiltration associated lncRNA

NCBI Gene: 100130111ENSG00000256802
56
ClinVar variants
39
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— LCIIAR
📋
ClinVar Variants
39 Pathogenic / Likely Pathogenic· 14 VUS of 56 total submissions

Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

56 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic36
Likely Pathogenic3
VUS14
Likely Benign2
Conflicting1
36
Pathogenic
3
Likely Pathogenic
14
VUS
2
Likely Benign
1
Conflicting

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————36
Likely Pathogenic
————3
VUS
————14
Likely Benign
————2
Benign
————0
Conflicting
—1
Total—56

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

LCIIAR · 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
Key Publications
Landmark & review papers · by relevance
PubMed
Top 10 resultsSearch PubMed ↗
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC
Top 5 resultsSearch Europe PMC ↗

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