TRBV19

Chr 7

T cell receptor beta variable 19

Also known as: TCRBV17S1A1T, TCRBV19S1

Predicted to be involved in cell surface receptor signaling pathway. Part of alpha-beta T cell receptor complex. [provided by Alliance of Genome Resources, Jul 2025]

0
Active trials
21
Pathogenic / LP
28
ClinVar variants
1
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryTRBV19
📋
ClinVar Variants
21 Pathogenic / Likely Pathogenic· 2 VUS of 28 total submissions

Population Genetics & Constraint

Constraint data not available from gnomAD.

DNGOF
DN
0.78top 25%
GOF
0.77top 25%
LOF
0.2289th %ile

This gene has evidence for multiple mechanisms of pathogenicity (dominant-negative and gain-of-function). Both the Badonyi & Marsh prediction and the broader genomic evidence point to dominant-negative as the predominant mechanism. Different variants in this gene may act through different mechanisms — interpret in context of the specific variant.

DNprediction above median
GOFprediction above median

Note: In-silico variant effect predictors (SIFT, PolyPhen, REVEL, CADD) may underestimate pathogenicity of missense variants in genes with GOF or DN mechanisms. Consider functional evidence and clinical context.

Predictions from Badonyi M, Marsh JA. PLoS ONE. 2024;19(8):e0307312.

ClinVar Variant Classifications

28 submitted variants in ClinVar

Classification Summary

Pathogenic20
Likely Pathogenic1
VUS2
Likely Benign5
20
Pathogenic
1
Likely Pathogenic
2
VUS
5
Likely Benign

Curated Variants Distribution

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

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
20
Likely Pathogenic
1
VUS
2
Likely Benign
5
Benign
0
Total28

Counts from ClinVar esearch · Updated hourly

View in ClinVar →

TRBV19 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

Search ClinicalTrials.gov →
Clinical Literature
Landmark / reviewRecent case evidence
Recent Gene-Specific Literature
Gene in title · MEDLINE · newest first
Europe PMC

No open access results found