Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE MYD88 p.L265P and CD79B p.Y196C/H mutations were analyzed in diffuse large B-cell lymphoma (DLBCL) patients whose tumor samples were available (N = 29). 31436356

2019

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE High frequencies of the hotspot <i>MYD88</i>(L265P) mutation are observed in extranodal diffuse large B-cell lymphoma and Waldenström macroglobulinemia, thereby demonstrating this mutation's potential as a disease marker. 31699794

2019

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE MYD88 L265P is the most common mutation in lymphoplasmacytic lymphoma/Waldenström macroglobulinemia (LPL/WM) and one of the most frequent in poor-prognosis subtypes of diffuse large B-cell lymphoma (DLBCL). 31698464

2019

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE <i>Results</i>: MYD88 L265P mutations were detected in 22 of 29 samples from 14 patients with diffuse large B-cell lymphomas and one patient with lymphoplasmacytoid lymphoma. 31603365

2019

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE ST2825 has the potential for clinical use in patients with L265P DLBCL, and other B‑cell neoplasms driven by activated MYD88 signaling. 31432184

2019

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Recent studies demonstrated that in the activated B cell subtype of diffuse large B cell lymphoma (DLBCL), approximately one-third of the patients harbored somatically acquired MyD88 L265P mutation in their lymphomas. 30253331

2018

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE A missense mutation (L265P) changing leucine at position 265 to proline in MYD88 is found in ∼90% of Waldenström macroglobulinemia (WM) cases and in significant portions of activated B-cell diffuse large B-cell lymphomas and IgM monoclonal gammopathy of undetermined significance. 29703722

2018

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Lack of a Prognostic Impact of the MyD88 L265P Mutation for Diffuse Large B Cell Lymphoma Patients Undergoing Autologous Stem Cell Transplantation. 28847710

2017

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Primary DLBCL in sanctuary sites (DLBCL-SS) also demonstrates these features, and >70% of patients harbor myeloid differentiation primary response 88 (MYD88) (L265P) and CD79B mutations. 27915469

2017

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Notably, the MYD88 L265P mutation rates of CNS and testicular DLBCL patients were 60% and 77%, respectively. 28496180

2017

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Finally, although the MYD88 L265P variant was not an independent prognostic factor in ABC DLBCL, associated <i>CD79B</i> mutations significantly improved the survival of MYD88 L265P-mutant ABC DLBCL in our cohort.<b>Conclusions:</b> This study highlights the relative heterogeneity of <i>MYD88</i>-mutant DLBCL, adding to the field's knowledge of the theranostic importance of <i>MYD88</i> mutations, but also of associated alterations, emphasizing the usefulness of genomic profiling to best stratify patients for targeted therapy.<i></i>. 27923841

2017

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE We identified the MYD88 L265P somatic variant in cases with WM (39/42), MGUS (8/18), NHL (14/41, including 4/13 diffuse large B cell lymphoma (DLBCL), 1/8 mucosa-associated lymphoid tissue, 3/6 splenic marginal zone lymphoma (SMZL), 1/4 chronic lymphocytic leukemia, 2/3 nodal marginal zone lymphoma (NMZL), 1/2 mantle cell lymphoma, 1 Burkitt lymphoma, and 1 B cell NHL that could not be classified), primary AL (2/2), and IgM-PN (1/1). 28280994

2017

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Also, MYD88 L265P had little involvement in GI DLBCL compared with other extranodal DLBCLs, suggesting that its pathogenesis might be different from that of organs with a high frequency of MYD88 L265P. 27439595

2016

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE B-cell-specific conditional expression of Myd88p.L252P leads to the development of diffuse large B-cell lymphoma in mice. 27048211

2016

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Myd-88 L265P constitutive activating mutations are present in at least some cases of the diffuse large B-cell lymphoma form of vitreoretinal lymphoma. 25768255

2015

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE The L265P mutation may be helpful for understanding the pathogenesis of immune-privileged site-associated DLBCLs. 25978699

2015

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE In conclusion, we demonstrated a high prevalence of the non-GCB subtype and the common MYD88 L265P in both primary and secondary testicular DLBCL. 26388135

2015

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE Heterozygous MYD88 L265P mutations were identified in 11 (9.2%) DLBCL cases, all of which were diagnosed as non-germinal-center B cell (non-GCB) DLBCL. 23178471

2013

dbSNP: rs387907272
rs387907272
0.100 GeneticVariation BEFREE MYD88 L265P</span> mutation was found in 6.5% (8/124) of DLBCL cases. 23380077

2013