LL22NC01-81G9.3

Chr 22

uncharacterized protein FLJ39582-like

NCBI Gene: 100506241ENSG00000215403
6
ClinVar variants
5
Pathogenic / LP
—
pLI score
0
Active trials
Clinical Summary— LL22NC01-81G9.3
📋
ClinVar Variants
5 Pathogenic / Likely Pathogenic· 1 VUS of 6 total submissions
Some data sources returned errors (1)

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Population Genetics & Constraint

gnomAD

Constraint data not available from gnomAD.

ClinVar Variant Classifications

6 submitted variants in ClinVar

ClinVar

Classification Summary

Pathogenic5
VUS1
5
Pathogenic
1
VUS

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
————5
Likely Pathogenic
————0
VUS
————1
Likely Benign
————0
Benign
————0
Total—6

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

LL22NC01-81G9.3 · 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 LL22NC01-81G9.3

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