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rdmorin edited this page Jan 11, 2025 · 32 revisions

bibliography: 'morinlab.bib' csl: 'NLM.csl' link-citations: true nocite: | @arthurGenomewideDiscoverySomatic2018,

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Overview

GRHPR 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. The mutation pattern in DLBCL implies the preferential accumulation of inactivating mutations. Coding and non-coding mutations in GRHPR are a feature of the MCD genetic subgroup of DLBCL.[@arthurGenomewideDiscoverySomatic2018] Further research is needed to elucidate the specific role of GRHPR mutations in DLBCL.

Relevance tier by entity

include:tables/table1_GRHPR.md

Mutation incidence in large patient cohorts (GAMBL reanalysis)

DLBCL

include:tables/DLBCL_GRHPR.md

Mutation pattern and selective pressure estimates

include:tables/dnds_GRHPR.md

aSHM regions

chr_name hg19_start hg19_end region regulatory_comment
chr9 37423010 37425279 TSS active_promoter

include:tables/browser_GRHPR.md

Expression

include:tables/mermaid_GRHPR.md

References

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