HNRNPU
Overview
HNRNPU is one of a number of genes affected by aberrant somatic hypermutation in B-cell lymphomas, which complicates the interpretation of mutations at this locus.
Relevance tier by entity
| Entity | Tier | Description |
|---|---|---|
| BL | 1-a | aSHM target and high-confidence BL gene |
| DLBCL | 1-a | aSHM target and high-confidence DLBCL gene |
Mutation incidence in large patient cohorts (GAMBL reanalysis)
| Entity | source | frequency (%) |
|---|---|---|
| BL | GAMBL genomes+capture | 5.77 |
| BL | Thomas cohort | 6.40 |
| BL | Panea cohort | 8.90 |
| DLBCL | GAMBL genomes | 2.49 |
| DLBCL | Schmitz cohort | 3.40 |
| DLBCL | Reddy cohort | 2.40 |
| DLBCL | Chapuy cohort | 3.42 |
Mutation pattern and selective pressure estimates
| Entity | aSHM | Significant selection | dN/dS (missense) | dN/dS (nonsense) |
|---|---|---|---|---|
| BL | Yes | Yes | 1.081 | 27.052 |
| DLBCL | Yes | No | 1.712 | 0.000 |
| FL | Yes | No | 4.865 | 31.056 |
aSHM regions
| chr_name | hg19_start | hg19_end | region | regulatory_comment |
|---|---|---|---|---|
| chr1 | 245023502 | 245029083 | TSS | NA |
[!NOTE] First described in BL in 2019 by Panea RI
## HNRNPU Hotspots
| Chromosome | Coordinate (hg19) | ref>alt | HGVSp |
|---|---|---|---|
| chr1 | 245027102 | G>A | Q170* |
| chr1 | 245027099 | G>C | Q171E |
| chr1 | 245027099 | G>A | Q171* |
View coding variants in ProteinPaint hg19 or hg38
View all variants in GenomePaint hg19 or hg38


