LNCARSR

Chr 9

lncRNA regulator of Akt signaling associated with HCC and RCC

Also known as: lnc-TALC

I cannot provide a clinical summary for LNCARSR as no information about this gene's protein function, associated diseases, or inheritance pattern was provided in the data below the instructions. To write an accurate clinical summary following the strict rules, I would need specific information about what protein this gene encodes, what diseases result from mutations, and the inheritance pattern.

Clinical SummaryLNCARSR
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ClinVar Variants
15 unique Pathogenic / Likely Pathogenic· 1 VUS of 16 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

16 submitted variants in ClinVar

Classification Summary

Pathogenic15
VUS1
15
Pathogenic
1
VUS

Curated Variants Distribution

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

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

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

LNCARSR · 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
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